Jobs at Click Therapeutics
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Accounting Manager - R&D (Hybrid)
Company: 4D Molecular Therapeutics - (4DMT)
Location: Other US Location
Posted Mar 16, 2024
<div> <p><em><strong>Attention recruitment agencies<strong> All agency inquiries are vetted through Talent Acquisition No unsolicited resumes will be accepted Agencies must be expressly engaged by the 4DMT talent acquisition team on any requisition Agencies reaching out directly to hiring managers will not be tolerated and may impact your ability to work with 4DMT in the future<em><p> <p><br ><p><p>4DMT is a clinicalstage biotherapeutics company harnessing the power of directed evolution for targeted genetic medicines We seek to unlock the full potential of gene therapy using our platform Therapeutic Vector Evolution TVE which combines the power of directed evolution with our approximately one billion synthetic AAV capsidderived sequences to invent evolved vectors for use in our products We believe key features of our targeted and evolved vectors will help us create targeted product candidates with improved therapeutic profiles These profiles will allow us to treat a broad range of large market diseases unlike most current genetic medicines that generally focus on rare or small market diseases <p> <p>We have built a deep portfolio of AVVbased gene therapy product candidates with five product candidates in clinical trials 4D150 for the treatment of wet agerelated macular degeneration wet AMD and diabetic macular edema DME 4D710 for the treatment of cystic fibrosis lung disease 4D310 for the treatment of Fabry disease cardiomyopathy 4D125 for the treatment of Xlinked retinitis pigmentosa XLRP and 4D110 for the treatment of choroideremia In addition we have two product candidates in preclinical studies 4D175 for geographic atrophy GA and 4D725 for alpha1 antitrypsin deficiency<p> <p>Todate we have demonstrated clinical proofofconcept for three evolved vectors in three therapeutic areas and routes of administration with five products and patient populations We believe this validates the power of our directed evolution platform for discovering superior vectors compared to wildtype viral vectors We have built a robust and efficient product engine with 6 open Investigational New Drug Applications INDs in the US 1 IND in Taiwan and 1 Clinical Trial Approval CTA in Australia We believe we are positioned to create develop manufacture and if approved effectively commercialize targeted genetic medicines that could transform the lives of patients suffering from debilitating diseases<p> <p>In addition to TVE our technology includes a robust AAV manufacturing platform and onsite manufacturing facility that allows us to rapidly produce and test research grade material and scale up to GMP clinical material This internal capability and close collaboration between our RampD and Manufacturing teams has greatly accelerated the pace of discovery at 4DMT<p> <p>Company Differentiators <p> <p> Fully integrated clinicalphase company with internal manufacturing<br > Demonstrated ability to move rapidly from idea to IND<br > Five candidate products in the clinic and two declared preclinical programs<br > Robust technology and IP foundation including our TVE and manufacturing platforms<br > Initial product safety and efficacy data substantiates the value of our platforms<br > Opportunities to expand to other indications and modalities within genetic medicine<p> <div> <p><span datacontrast=auto>GENERAL SUMMARY<span><span dataccpprops=> <span><p> <p><span datacontrast=auto>The Accounting Manager RampD will join the finance and accounting team working with multiple crossfunctional teams including but not limited to clinical and preclinical RampD and technical operationsCMC The ideal candidate will be handson and responsible for managing clinical trial program and functional budgets preparing detailed accruals and reviewing and analyzing contracts<span><span dataccpprops=> <span><p> <p><span dataccpprops=>This is a Hybrid role requiring 13 days a week in office work Bay Area based candidates required<span><p> <p><span datacontrast=auto>RESPONSIBILITIES <span><span dataccpprops=> <span><p> <ul><li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=1 dataarialevel=1><span datacontrast=auto>Partner with our Clinical FPampA CMC and Research teams to ensure completeness and accuracy of Clinical Trials expenses<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=2 dataarialevel=1><span datacontrast=auto>Establish relationships with our external CROs and other Clinical Trial and CMC vendors to ensure accurate and timed monthly reporting<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=3 dataarialevel=1><span datacontrast=auto>Work closely with the clinical and procurement team to ensure all executed RampD contracts have been entered as purchase orders in the ERP<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=4 dataarialevel=1><span datacontrast=auto>Review and track Clinical Trials and CMC agreements<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=5 dataarialevel=1><span datacontrast=auto>Assist with the monthend close for Clinical and CMC including accruals prepayments recording journal entries and balance sheet accounts reconciliations<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=6 dataarialevel=1><span datacontrast=auto>Assist with trend and variance analysis for Clinical and CMC costs and balances<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=7 dataarialevel=1><span datacontrast=auto>Develop and maintain financial reports including monthly and quarterly financial packages with variance reporting to budget and prior periods<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=8 dataarialevel=1><span datacontrast=auto>Manage financial models for RampD pipeline programs to support decisionmaking and provide key insights<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=9 dataarialevel=1><span datacontrast=auto>Ensure compliance with SOX policies and procedures<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=10 dataarialevel=1><span datacontrast=auto>Assist with external audit requests and PBC items for quarterly and yearend audits<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=11 dataarialevel=1><span datacontrast=auto>Participate in other adhoc projects and analyses as needed Other duties as assigned nothing in this job description restricts managements right to assign or reassign duties and responsibilities to this job at any time<span><span dataccpprops=> <span><li> <ul><p><span datacontrast=auto>QUALIFICATIONS<span><span dataccpprops=> <span><p> <p><span datacontrast=auto>Education<span><span dataccpprops=> <span><p> <ul><li dataleveltext= datafont=Symbol datalistid=8 datalistdefnprops= dataariaposinset=12 dataarialevel=1><span datacontrast=auto>Minimum bachelors degree with a business finance or accounting major<span><span dataccpprops=> <span><li> <ul><p><span datacontrast=auto>Experience<span><span dataccpprops=> <span><p> <ul><li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=13 dataarialevel=1><span datacontrast=auto>5 7 years of accounting experience in the biotechnologypharmaceutical industry<span><span dataccpprops=> <span><li> <ul><p><span datacontrast=auto>Skills<span><span dataccpprops=> <span><p> <ul><li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=1 dataarialevel=1><span datacontrast=auto>Proficiency with Excel to organize and analyze data<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=2 dataarialevel=1><span datacontrast=auto>Strong timemanagement skills and ability to prioritize and multitask<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=3 dataarialevel=1><span datacontrast=auto>Selfstarter attitude with the ability to approach challenges and urgent requests with a positive problemsolving mindset<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=4 dataarialevel=1><span datacontrast=auto>Strong interpersonal verbal and written communication skills<span><span dataccpprops=> <span><li> <li dataleveltext= datafont=Symbol datalistid=5 datalistdefnprops= dataariaposinset=5 dataarialevel=1><span datacontrast=auto>Ability to build and maintain strong working relationships<span><li> <ul><p>Base salary compensation range<p> <p>Bay Area Range $109000yr $134000yr<p> <p>Please note the base salary compensation range and actual salary offered to the final candidate depends on various factors candidates geographical location relevant work experience skills and years of experience<p> <div> <p>4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race color religion gender sexual orientation national origin age disability genetic information marital status status as a covered veteran and any other category protected under applicable federal state provincial and local laws<p> <p> <p> <p>Equal Opportunity EmployerProtected VeteransIndividuals with Disabilities<p> <div>
Manager/Sr. Manager, Market Access Data Science
Company: Axsome Therapeutics, Inc.
Location: New York City, NY
Posted Mar 15, 2024
<p>Axsome Therapeutics Inc is a biopharmaceutical company developing and delivering novel therapies for the management of central nervous system CNS disorders The Axsome team is a lean dynamic group of individuals committed to addressing unmet needs for patients with CNS disorders Axsome is based in New York City<p> <p><strong>About This Role<strong><p> <p>Axsome Therapeutics is seeking a Senior Manager Market Access Data Science to lead and oversee the technical implementation of datadriven solutions and strategies that support Market Access objectives This position will play a crucial role in translating insights from key subject matter experts into actionable data analytics solutions and fostering crossfunctional collaboration to drive superior market insights and strategies<p> <p><em>This role is based at Axsomes HQ in New York City<em><p> <p><strong>Job Responsibilities and Duties<strong> include but are not limited to the following<p> <p>Data Warehousing<p> <ul><li>Collaborate with IT to identify the most appropriate data servers eg AWS Azure et all for different needs ensuring optimal performance integration and costefficiency<li> <li>Develop and maintain a robust archive for internal data use ensuring data integrity security and ease of retrieval<li> <li>Support audit processes by ensuring timely and accurate data extraction<li> <li>Assist in strategy development and informative analytics by providing a consolidated view of all relevant data points<li> <ul><p>Data Reporting<p> <ul><li>Handson technical design and generation of foundational executivelevel internal team and crossfunctional reports to inform decisionmaking<li> <li>Actively collaborate with key subject matter experts to understand reporting needs and ensure alignment<li> <li>Expertly utilize tools like PowerBI and Tableau to craft insightful and actionable reports catering to both technical and nontechnical audiences<li> <li>Partner with IT to establish secure and compliant data transfer protocols for reporting purposes adhering to best practices in data governance and internal Axsome data governance policies<li> <ul><p>Model Development<p> <ul><li>Be proactive in the handson development of predictive analytic models emphasizing accurate forecasting of key metrics including volume market share and class size<li> <li>Collaborate closely with subject matter experts to understand the business context and tailor models to specific needs and deliverables<li> <li>Implement and optimize deal analytics tools to better manage chargebacks and returns ensuring operational efficiency and revenue accuracy<li> <li>Ensure that all models are underpinned by sound academic and practical theories as well as wellarticulated hypotheses Use forecasting methodologies that might include but arent limited to<li> <li>Drive technical analyses for deal or no deal evaluations contract strategy optimization and price strategy analytics<li> <ul><p>CrossFunctional Data Collaboration<p> <ul><li>Engage actively with IT to harmonize data strategies ensuring appropriate data server selection and utilization and compliance with data protection policies<li> <li>To ensure a comprehensive data approach facilitate collaboration within the broader Market Access team as well as with various internal departments including Commercial Operations Supply Chain and Finance<li> <li>Integrate diverse datasets to provide a holistic view of the market and optimize strategic initiatives<li> <ul><p><strong>Requirements Qualifications<strong><p> <ul><li>Masters degree in Data Science Biostatistics Computer Science or related STEM Field<li> <li>5+ years of relevant experience in data science Experience in biotechpharma commercialization preferred<li> <li>Ability to work on site Monday Tuesday amp Thursday<li> <ul><p><strong>Experience and Knowledge<strong><p> <ul><li>Experience in predictive analytics and statistical modeling software eg SAS R Python<li> <li>Proficiency in forecasting methodologies such as ARIMA exponential smoothing time series decomposition Familiarity with advanced machine learning algorithms for predictive modeling<li> <li>Proficiency in cloudbased data server management AWS Azure Google Cloud<li> <li>Strong understanding of data integration ETL tools such as Talent Informatica or SSIS<li> <li>Expertise in data visualization tools like PowerBI Tableau<li> <li>Familiarity with SQL and data extraction methodologies<li> <li>Knowledge of data governance and compliance standards eg HIPAA for healthcare data<li> <li>Ability to integrate diverse datasets using programming languages like R or Python<li> <li>Strong collaborative skills to work with IT Commercial Operations Supply Chain and Finance<li> <ul><p><strong>Salary amp Benefits<strong><p> <p>The anticipated salary range for this role is $125000 $140000 We encourage candidates of all levels to apply as there may be flexibility on final job title and responsibilities The salary offer will be based on a variety of factors including experience qualifications internal equity and location Axsome offers a competitive employment package that includes an annual bonus significant equity and a generous benefits package<p> <p><em>Axsome Therapeutics does not accept unsolicited resumes from recruiters or thirdparty recruitment agencies and will not pay placement fees for unsolicited candidates that are sent to hiring managers the HR team or other Axsome team members Only approved vendors who have been explicitly asked to support a specific search will receive access to our Applicant Tracking System to submit candidates for consideration <em><p>
Manager, Human Resources
Company: Halozyme Therapeutics
Location: San Diego, CA
Posted Mar 16, 2024
The job posting is for a Manager, Human Resources position at Halozyme, a company that is reinventing the patient experience and building the future of drug delivery. The role involves leading HR operations, benefits administration, and leave of absence management, and requires a balance of analytical, detail-oriented work and strategic problem-solving. The ideal candidate will be a self-starter who can drive process improvements, streamline operations, and maintain compliance with company policies and legal regulations.
Senior Manager, Market Research and Competitive Intelligence
Company: Axsome Therapeutics, Inc.
Location: New York City, NY
Posted Mar 15, 2024
<p><span datacontrast=none>Axsome Therapeutics Inc is a biopharmaceutical company developing and delivering novel therapies for the management of central nervous system CNS disorders The Axsome team is a lean dynamic group of individuals committed to addressing unmet needs for patients with CNS disorders Axsome is based in New York City<span><p> <p><strong><span datacontrast=none>About This Role<span><strong><span dataccpprops=> <span><p> <p><span datacontrast=none>Axsome Therapeutics is hiring a Senior Manager Market Research and Competitive Intelligence to provide vital expertise to the commercial organization Responsibilities include leading competitive intelligence CI insight generation through primary market research qualitative and quantitative monitoring of competitor activities analyzing market trends and assessing clinical timelines This position will work directly with the commercial leadership team Marketing Sales Value amp Access in planning budgeting directing and executing all initiatives in support of commercialization strategies for key products This critical role will report directly to the Associate Director of Market Research<span><span dataccpprops=> <span><p> <p><em><span datacontrast=none>This role is based at Axsomes HQ in New York City with an onsite requirement of at least three days per week <span><em><span dataccpprops=> <span><p> <p><strong><span datacontrast=none>Job Responsibilities and Duties<span><strong><span datacontrast=none> include but are not limited to the following<span><span dataccpprops=> <span><p> <ul><li dataleveltext=● datafont=Noto Sans Symbols datalistid=3 datalistdefnprops= sans= symbols= dataariaposinset=1 dataarialevel=1><span datacontrast=none>Develop and execute CI strategies to identify market opportunities and risks<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=3 datalistdefnprops= sans= symbols= dataariaposinset=2 dataarialevel=1><span datacontrast=none>Provide thought leadership and subject matter expertise in CI and strategic analytics<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=3 datalistdefnprops= sans= symbols= dataariaposinset=3 dataarialevel=1><span datacontrast=none>Build and maintain a CI repository of indepth analyses of key competitors including commercial strategies current and prospective timelines market positioning clinical assessment and lifecycle management<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=3 datalistdefnprops= sans= symbols= dataariaposinset=4 dataarialevel=1><span datacontrast=none>Translate and synthesize disparate data research and analyses into actionable compelling insights that deepen competitive and market understanding across the organization<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=3 datalistdefnprops= sans= symbols= dataariaposinset=5 dataarialevel=1><span datacontrast=none>Facilitate dissemination of timely CI insights throughout the organization ensuring insights are aligned to business objectives and provide clear recommendations<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=3 datalistdefnprops= sans= symbols= dataariaposinset=6 dataarialevel=1><span datacontrast=none>Ensure continuous alignment and strategic partnership with Marketing Sales Market Access Medical Affairs Corporate Communications and Executive Leadership<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=3 datalistdefnprops= sans= symbols= dataariaposinset=7 dataarialevel=1><span datacontrast=none>Support market research initiatives focusing on understanding the competitive landscape market trends and customer needs<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=3 datalistdefnprops= sans= symbols= dataariaposinset=8 dataarialevel=1><span datacontrast=none>Identify evaluate and manage relationships with bestinclass competitive intelligence vendors<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=3 datalistdefnprops= sans= symbols= dataariaposinset=1 dataarialevel=1><span datacontrast=none>Ensure that all projects comply Axsomes SOPs and CI policy Ensure all projects adhere to industry standards eg SCIP and operate to the highest professional standard and meet expectations on quality timeliness and budget<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=3 datalistdefnprops= sans= symbols= dataariaposinset=2 dataarialevel=1><span datacontrast=none>Travel required about 4 to 6 weeks in the year for attending medical conferences<span><span dataccpprops=> <span><li> <ul><p><strong><span datacontrast=none>Requirements Qualifications<span><strong><span dataccpprops=> <span><p> <ul><li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=3 dataarialevel=1><span datacontrast=none>Bachelors degree required<span><span dataccpprops=> <span>Advanced degree including MBA or Masters in related field preferred<li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=3 dataarialevel=1>5+ years pharmaceutical or biotech experience<li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=3 dataarialevel=1>35 years pharmaceutical or biotech CI or market research experience<li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=3 dataarialevel=1>Two or more years of CNS specific market research or competitive intelligence experience<li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=3 dataarialevel=1>Ability to work on site Monday Tuesday amp Thursday <em><span datacontrast=none>We are unable to consider candidates who are looking for fully remote roles <span><em><span datacontrast=none> <span><span dataccpprops=> <span><li> <ul><p><strong><span datacontrast=none>Experience and Knowledge<span><strong><span dataccpprops=> <span><p> <ul><li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=8 dataarialevel=1><span datacontrast=none>Expertise with competitive intelligence methodologies<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=9 dataarialevel=1><span datacontrast=none>Knowledge of secondary data sources used in pharmaceutical industry<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=10 dataarialevel=1><span datacontrast=none>Demonstrated exceptional strategic critical thinking abilities and business acumen<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=11 dataarialevel=1><span datacontrast=none>Demonstrated analytical skills understands the advantages and limits of different analyticalquantitative approaches<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=12 dataarialevel=1><span datacontrast=none>Familiarity with launch and prelaunch timelines strategies and planning<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=13 dataarialevel=1><span datacontrast=none>Familiarity with direct to HCP Consumer and Payer strategies and tactics<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=1 dataarialevel=1><span datacontrast=none>Familiarity with clinical trial protocols and timelines<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=2 dataarialevel=1><span datacontrast=none>Excellent oral written and presentation skills with ability to explain complex concepts clearly to a variety of audiences including Executive Leadership<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=3 dataarialevel=1><span datacontrast=none>Ability to work collaboratively in teambased environment<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=4 dataarialevel=1><span datacontrast=none>Ability to balance multiple projects and workstreams simultaneously<span><span dataccpprops=> <span><li> <li dataleveltext=● datafont=Noto Sans Symbols datalistid=1 datalistdefnprops= sans= symbols= dataariaposinset=5 dataarialevel=1><span datacontrast=none>Additional skillsqualifications for the role including any that are preferred but not required<span><span dataccpprops=> <span><li> <ul><p><strong><span datacontrast=none>Salary amp Benefits <span><strong><span dataccpprops=> <span><p> <p><span datacontrast=none>The anticipated salary range for this role is $135000 $155000 We encourage candidates of all levels to apply as there may be flexibility on final job title and responsibilities The salary offer will be based on a variety of factors including experience qualifications internal equity and location Axsome offers a competitive employment package that includes an annual bonus significant equity and a generous benefits package<span><span dataccpprops=> <span><p> <p><em><span datacontrast=none>Axsome is committed to equal employment opportunity and providing reasonable accommodations to applicants with physical andor mental disabilities We value and encourage diversity and solicit applications from all qualified applicants without regard to race color gender sex age religion creed national origin sexual orientation gender identity ancestry citizenship marital status physical or mental disability medical condition veteran status genetic information or any other characteristic protected by federal state or local law<span><em><span dataccpprops=> <span><p> <p><em>Axsome Therapeutics does not accept unsolicited resumes from recruiters or thirdparty recruitment agencies and will not pay placement fees for unsolicited candidates that are sent to hiring managers the HR team or other Axsome team members Only approved vendors who have been explicitly asked to support a specific search will receive access to our Applicant Tracking System to submit candidates for consideration <em><p>
Data Privacy Intern
Company: Click Therapeutics
Location: New York City, NY
Posted Mar 15, 2024
<p><strong>Who We Are<strong><br >Click Therapeutics Inc develops validates and commercializes software as prescription medical treatments for people with unmet medical needs As a leading innovator of Digital Therapeutics™ Click delivers accessible clinically proven FDAregulated prescription treatments to the smartphone in your hand Clicks treatments are defined by a commitment to applying technical and scientific rigor and patientcentric design to the development process This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options Click Therapeutics continuously expands and refines its platform with novel cognitive behavioral and neuromodulatory mechanisms of action and advanced datadriven tools such as artificial intelligence and machine learning The digital therapeutics under development on Clicks platform address diverse areas of therapeutic need including indications in psychiatry neurology oncology immunology and cardiometabolic diseases Consistently named a best place to work Click fosters an inclusive diverse workforce of innovators clinicians scientists researchers designers technologists engineers and more united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics For more information visit wwwclicktherapeuticscom and connect with us on LinkedIn <br ><strong>About the Role<strong><br >We are currently seeking a Data Privacy Intern to join our dynamic privacy team This internship offers a unique opportunity to delve into various privacy functions policies and procedures enabling you to actively contribute to the overall achievements of both the privacy department and the organization Collaborating closely with our experienced privacy professionals you will gain valuable insights into all things privacy<br >This position is based out of Clicks headquarters located in Tribeca NYC at the center of one of the fastestgrowing digital health communities This is a hybrid internship in which you will come to the office Tuesday and Thursday <br ><strong>Responsibilities<strong><br ><p><ul><li>Create data privacy policies and procedures for the privacy compliance program that uphold the highest standards <li> <li>Partner with internal functional teams to ensure compliance with HIPAA as well as state national and international data privacy regulations and laws<li> <li>Assist with crossdepartment privacy initiatives with Cybersecurity Technology Development Product Management Commercial Science Medical Office and HR<li> <li>Support the privacy training program to teach colleagues about Clicks privacy compliance program and best practices for handling personal information <li> <li>Coordinate and enable compliance monitoring activities including reporting and analytics<li> <li>Identify data privacy concerns with respect to new initiatives and the use of new technologies eg privacy risks associated with data processing utilizing AI and propose mitigation strategies<li> <li>Support additional special projects on an Adhoc basis<li> <ul><p> <br ><strong>Qualifications<strong><br ><p><ul><li>Rising Junior or Senior undergrad<li> <li>Experience developing and writing policies standard operating procedures Privacy Impact Assessments or other technical writing <li> <li>Ability to collaborate effectively with a diverse set of key stakeholders including data privacy counsel in communicating regulatory guidance <li> <li>Superior verbal and written communication skills with the ability to construct clear and concise analyses <li> <li>Strong organizational skills with the ability to balance short and longterm project deadlines in a fastpaced environment <li> <li>Handson experience acquired through internships jobs research or personal projects<li> <li>Must be excited to learn through a combination of onthejob and independent learning<li> <ul><p> <br ><strong>Preferred Qualifications<strong><br ><p><ul><li>Experience with OneTrust TrustArc or another privacy management software<li> <li>Understanding of AI algorithms and the intersection with privacy concerns<li> <ul><p> <br ><strong>Compensation<strong> $22hr <br ><strong>Hours and Duration <strong><br >This is a parttime 30 hoursweek position The internship will have a duration of 11 weeks from May 15th July 26th 2024 <br ><strong>Benefits<strong><br >Mac Laptop | Grubhub | Sponsored Company Events | Unlimited Office Snacks and Beverages | Much More <br ><strong>Equal Employment Opportunity<strong><br >Click Therapeutics is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race color religion sex sexual orientation age gender identity or gender expression national origin disability or veteran status Click Therapeutics also complies with all applicable national state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act All applicants must have authorization to work for Click Therapeutics in the US In certain circumstances it may be advantageous to Click Therapeutics to support the applications for temporary visa classification andor sponsor applications for permanent residence so that a foreign national colleague can accept or remain in a work assignment in the U S For certain classes of temporary visas the resulting work authorization may be specific to Click Therapeutics and the specific job andor work site Click Therapeutics may at its business discretion decide to or refrain from obtaining maintaining andor extending the temporary visa status andor sponsoring a colleague for permanent residency and or employment eligibility considering factors such as availability of qualified US workers and the colleagues longterm prospects for securing lawful permanent residence among other reasons Employment applicants requiring immigration sponsorship must disclose when initial application for employment is made whether or not they are legally authorized to work for Click Therapeutics in the US and if so whether that authorization permits them to work in the job they seek In no case should Click Therapeutics support of a colleagues temporary visa application or sponsorship of a colleague for permanent residence be construed to guarantee success of that application or amend or otherwise invalidate the atwill employment relationship between the colleague and Click Therapeutics <br ><strong>Recruitment Phishing Scams <strong><br >As recruitment phishing scams are growing we urge you to be vigilant during the job search process Please be mindful of the following<br ><p><ul><li> Click Therapeutics will only reach out to you through an clicktherapeuticscom email address <li> <li> Other than your email address or telephone number which you may provide via a job application portal Click Therapeutics will never ask you to provide personally identifiable information about yourself such as a Social Security Number or Drivers License Number via email or a messaging application like that used on the LinkedIn platform <li> <li> Click Therapeutics will conduct interviews facetoface over Zoom <li> <li> All job postings will be listed on the Click Therapeutics official career page If someone contacts you about a job or position that is not listed on the official career page please contact the Click Therapeutics recruitment team at the contact information below <li> <li> If you have any questions regarding the validity of a recruitment inquiry or an interview please contact the Clicks recruitment team at recruitmentclicktherapeuticscom to confirm before proceeding<li> <ul><p> <br >If you encounter a scam report it to the Federal Trade Commission at httpsreportfraudftcgov<p>
Associate Director, Pharmacology/Toxicology Study Monitor (Hybrid)
Company: 4D Molecular Therapeutics - (4DMT)
Location: Other US Location
Posted Mar 16, 2024
<div> <p><em><strong>Attention recruitment agencies<strong> All agency inquiries are vetted through Talent Acquisition No unsolicited resumes will be accepted Agencies must be expressly engaged by the 4DMT talent acquisition team on any requisition Agencies reaching out directly to hiring managers will not be tolerated and may impact your ability to work with 4DMT in the future<em><p> <p><br ><p><p>4DMT is a clinicalstage biotherapeutics company harnessing the power of directed evolution for targeted genetic medicines We seek to unlock the full potential of gene therapy using our platform Therapeutic Vector Evolution TVE which combines the power of directed evolution with our approximately one billion synthetic AAV capsidderived sequences to invent evolved vectors for use in our products We believe key features of our targeted and evolved vectors will help us create targeted product candidates with improved therapeutic profiles These profiles will allow us to treat a broad range of large market diseases unlike most current genetic medicines that generally focus on rare or small market diseases <p> <p>We have built a deep portfolio of AVVbased gene therapy product candidates with five product candidates in clinical trials 4D150 for the treatment of wet agerelated macular degeneration wet AMD and diabetic macular edema DME 4D710 for the treatment of cystic fibrosis lung disease 4D310 for the treatment of Fabry disease cardiomyopathy 4D125 for the treatment of Xlinked retinitis pigmentosa XLRP and 4D110 for the treatment of choroideremia In addition we have two product candidates in preclinical studies 4D175 for geographic atrophy GA and 4D725 for alpha1 antitrypsin deficiency<p> <p>Todate we have demonstrated clinical proofofconcept for three evolved vectors in three therapeutic areas and routes of administration with five products and patient populations We believe this validates the power of our directed evolution platform for discovering superior vectors compared to wildtype viral vectors We have built a robust and efficient product engine with 6 open Investigational New Drug Applications INDs in the US 1 IND in Taiwan and 1 Clinical Trial Approval CTA in Australia We believe we are positioned to create develop manufacture and if approved effectively commercialize targeted genetic medicines that could transform the lives of patients suffering from debilitating diseases<p> <p>In addition to TVE our technology includes a robust AAV manufacturing platform and onsite manufacturing facility that allows us to rapidly produce and test research grade material and scale up to GMP clinical material This internal capability and close collaboration between our RampD and Manufacturing teams has greatly accelerated the pace of discovery at 4DMT<p> <p>Company Differentiators <p> <p> Fully integrated clinicalphase company with internal manufacturing<br > Demonstrated ability to move rapidly from idea to IND<br > Five candidate products in the clinic and two declared preclinical programs<br > Robust technology and IP foundation including our TVE and manufacturing platforms<br > Initial product safety and efficacy data substantiates the value of our platforms<br > Opportunities to expand to other indications and modalities within genetic medicine<p> <div> <p>Purpose <p> <p>The primary purpose of the Associate Director PharmacologyToxicology Study Monitor is to support members of our research team in the initiation execution and management of nonclinical pharmacology and toxicology studies with contract research organizations CROs This position will work primarily with RampD teams in an office setting with hybrid andor remote opportunities <p> <p>This is a Hybrid role requiring 13 days a week in office work as needed Bay Area based candidates preferred<br > <p> <p>Essential Job Responsibilities <p> <ul><li>We seek an experienced innovative and teamoriented pharmtox study monitor that can take a significant role in the following activities <li> <li>Monitor in vivo pharmacologytoxicology studies in rodents and NHPs nonGLP and GLP <li> <li>Perform regular site visits at CROs for in vivo studies to ensure compliance to study protocols and procedures <li> <li>Management of preclinical study operations including sample shipment logistics and tracking of timelines and deliverables <li> <li>Maintain master study schedule for multiple ongoing PharmTox studies across research and development <li> <li>Assist in review of study documentation and results including QAQC of raw data <li> <li>Provide administrative support for nonclinical studies including integration of reported data into internal data management system <li> <li>Domestic travel to monitor studies at contract research organizations is required <li> <ul><p>Qualifications Required <p> <ul><li>4+ years relevant experience with PhD in a scientific discipline Pharmacology Toxicology Immunology etc with previous relevant experience in the management and operations of CRObased preclinical studies <li> <li>12+ years relevant experience with BSBA 8+ years relevant experience with MSMA <li> <li>Critical review of studyrelated documents protocols amendments and reports for completeness accuracy and consistency <li> <li>A comprehensive understanding of the conduct of nonclinical pharmacology and toxicology studies in nonhuman primates with a high attention to detail are important attributes for this role <li> <li>Understanding and knowledge of key scientific software programs including Microsoft Office and Prism <li> <li>Strong organizational skills analytical skills and problemsolving skills <li> <li>Willingness to learn and grow with enthusiasm to be part of the development of a cuttingedge gene therapy platform in multiple therapeutic areas <li> <ul><p> <p> <p>Preferred <p> <ul><li>Knowledge and handson experience in planning executing analysis and reporting of in vivo pharmacology andor toxicology studies is required Experience as a Study Director would be an advantage <li> <li>Experience with multiple species including NHPs is preferred Experience with the development of gene therapies is a plus <li> <li>Previous experience in the identification and management of external CROs <li> <li>Knowledge of global regulatory guidelines ICHGLPOECD and monitoring of GLPcompliant toxicology studies is a plus <li> <li>Adept at managing and executing multiple projects in a fastpaced and innovative research setting <li> <ul><p>Base salary compensation range<p> <p>Bay Area Range $166000yr $200000yr<p> <p>Please note the base salary compensation range and actual salary offered to the final candidate depends on various factors candidates geographical location relevant work experience skills and years of experience<p> <p><br ><br ><p><div> <p>4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race color religion gender sexual orientation national origin age disability genetic information marital status status as a covered veteran and any other category protected under applicable federal state provincial and local laws<p> <p> <p> <p>Equal Opportunity EmployerProtected VeteransIndividuals with Disabilities<p> <div>
VP, Head of Compliance
Company: Dyne Therapeutics
Location: Waltham
Posted Mar 15, 2024
<div><b>Company Overview<b> <p>Dyne Therapeutics is a clinicalstage muscle disease company focused on advancing innovative lifetransforming therapeutics for people living with genetically driven diseases With its proprietary FORCE™ platform Dyne is developing modern oligonucleotide therapeutics that are designed to overcome limitations in delivery to muscle tissue Dyne has a broad pipeline for serious muscle diseases including clinical programs for myotonic dystrophy type 1 DM1 and Duchenne muscular dystrophy DMD and a preclinical program for facioscapulohumeral muscular dystrophy FSHD For more information please visit httpswwwdynetxcom and follow us on X LinkedIn and Facebook <p> <div> <p><strong>Role Summary<strong><p> <p>In this role the Head of Compliance will design implement and administer a comprehensive compliance program appropriate to the size and stage of Dyne that is scalable as Dyne transitions to a commercial stage company The Head of Compliance also will act as the primary resource for healthcare law legal counseling across the entire organization The person in this role will work with our CEO and Board of Directors<p> <p>This role is based in Waltham MA without the possibility of being a remote role Applicants must be able to relocate to the area<p> <p><strong>Primary Responsibilities Include<strong><p> <ul><li>Responsible for establishment and leadership of an effective global healthcare compliance program<li> <li>Strategic compliance advisor to the Board of Directors and the management team<li> <li>Healthcare law and data privacy legal advisor to the entire company<li> <li>Responsible for the compliance program with respect to data privacyprotection antibribery and corporate compliance<li> <li>Senior member of the Legal amp Compliance team a highly visible representative for the team<li> <li>Design implement and maintain an effective global healthcare compliance program encompassing compliance with healthcare laws and ethical codes <ul><li>Engage employees management and Board with the compliance agenda its strategic importance to the business and its relationship to our values and goals<li> <li>Design implement administer and continuously improve an effective global healthcare compliance program including policies and procedures compliance committees training communication monitor and auditing enforcement and investigations<li> <li>Design implement and maintain system to check for excluded individualsentities<li> <li>Review and advise on publications promotional prepromotional materials presentations and agreements concerning dealings with Healthcare Professionals HCPs patients patient advocacy groups payors and reporting<li> <ul><li> <li>Responsible for the compliance program with respect to data privacyprotection antibribery and corporate compliance in partnership with other subject matter experts and functional leads<li> <li>Responsible for implementing and conducting price and transparency reporting<li> <li>Responsible for providing legal advice to the organization on precommercial and commercial healthcare law issues as well as data privacy issues<li> <li>Responsible for managing any external resources that may be required ensuring company receives highquality advice on time and on budget<li> <li>Stay connected across the business in a monitoring role to identify and proactively address compliance issues<li> <li>Support the Head of Legal in compliance and healthcare law matters as well as administrative matters<li> <li>Grow and mature the Compliance function and the Healthcare legal function<li> <ul><p><strong>Education and Skills Requirements<strong><p> <ul><li>JD from accredited law school and license to practice in at least one US jurisdiction compliance certification preferred<li> <li>Minimum of 15 years of experience in healthcare compliance and healthcare law preferably with experience in a clinicalstage biotechnology company and a toptier law firm<li> <li>Comprehensive knowledge of and experience in all US compliance topics<li> <li>Experience with compliance regimes outside of the US in major <em>ex<em>US markets<li> <li>Experience with data privacy <em>g<em> GDPR state privacy laws<li> <li>Experience in an inhouse role<li> <li>Experience interacting with a management team andor a Board of Directors<li> <li>Experience in the design and implementation of a healthcare compliance program for a growing biotechnology company<li> <li>Proven selfstarter and multitasker in a fastpaced environment<li> <li>Excellent communication writing and computer skills<li> <li>Ability to collaborate well with internal and external stakeholders<li> <li>Excellent analytical organizational and informationseeking skills detail oriented<li> <li>Exceptional business judgment with the ability to think strategically and give practical advice while balancing business needs with legal risks<li> <ul><p>LIOnsite<p> <div> <p>The statements contained herein reflect general details as necessary to describe the principles functions for this job the level of knowledge and skill typically required and the scope of responsibility but should not be considered an allinclusive listing of work requirements Individuals may perform other duties as assigned including work in other functional areas to cover absences or relief to equalize peak work periods or otherwise balance workload<p> <p>This description is not intended to be constructed as an exhaustive list of duties responsibilities or requirements for the position This position may change or assume additional duties at any time The employee may be requested to perform different or additional duties as assigned All Employees are expected to adhere to all company policies and act as a role model for company values<p> <p><em><span>Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age color disability gender national origin race religion sexual orientation veteran status or any classification protected by federal state or local law<span><em><p> <div>
Research Associate I / Research Associate II, Analytical Development
Company: Capstan Therapeutics
Location: San Diego, CA
Posted Mar 15, 2024
<p><span><span><span><span><b><span><span>About Capstan Therapeutics<span><span><b><span><span><span><span><br ><span><span><span><span><span><span>Capstan Therapeutics Inc is a privately held biotechnology company dedicated to advancing in vivo cell reprogramming The core platform technology comprises proprietary targeted lipid nanoparticles tLNPs that are composed of LNPs conjugated with a recombinant protein binder such as a monoclonal antibody tLNPs are designed to deliver payloads including mRNA or gene editing tools capable of reprogramming specific cell types in vivo The platform technology has the potential to generate transformative therapies with possible applications across a broad range of disease areas including oncology autoimmune disorders fibrosis and monogenic blood disorders<span><span><span><span><span><span><br ><span><span><span><b><span><span><span>The Opportunity<span><span><span><b><br ><span><span><span>Capstan is seeking <span><span><span><span><span>a highly motivated Research Associate I or Research Associate II to join the Analytical Development<span><span><span><span><span> team In this role you will be responsible for routine testing along with analytical method developmentoptimization for characterization of our LNPstLNPs along with its individual components This role requires a strong attention to detail with a quantitativeanalytical mindset and drive to tackle complex problems in a dynamic environment<span><span><span><span><span><span><br ><span><span><span><b><span><span>Responsibilities amp Duties<span><span><b><span><span><span> <p><ul><li><span><span><span><span><span>Perform routine analysis and participate in developmentoptimization of methods as outlined by supervisor to characterize LNPstLNPs along with their individual components<span><span><span><span><span><li> <li><span><span><span><span><span>Follow safety proceduresguidelines protocols and Standard Operating Procedures SOPs<span><span><span><span><span><li> <li><span><span><span><span><span>Maintain detailed and comprehensive documentation and electronic lab notebook ELN entries for all performed experiments and assays<span><span><span><span><span><li> <li><span><span><span><span><span>Prepare reports and presentations summarizing results and data interpretation as needed<span><span><span><span><span><li> <li><span><span><span><span><span>Collaborate with internal and crossfunctional teams to ensure accuracy and reliability of data output in addition to troubleshooting out of trend results<span><span><span><span><span><li> <li><span><span><span><span><span>Participate in team meetings to discuss methodsdata in addition to contributing insights and suggestions for any improvements to operations analytical procedures methods SOPs etc<span><span><span><span><span><li> <li><span><span><span><span><span>Support analytical lab operations through equipment maintenance organizing and maintaining inventory aliquoting and labeling and other tasks as needed <span><span><span><span><span><li> <ul><p><span><span><span><b><span><span>RequirementsQualifications<span><span><b><span><span><span> <p><ul><li><span>Typically candidates possess a bachelors degree or equivalent coupled with 0 to 2+ years of relevant industry experience<span><li> <li><span><span><span><span><span>Bachelors degree in Analytical Chemistry Chemistry Biochemistry Pharmaceutical Sciences or other related scientific field is preferred<span><span><span><span><span><li> <li><span><span><span><span><span>Additional advantage for candidates with proficiency in any of the following<span><span><span><span><span><br ><ul><li><span><span><span><span><span>HighPerformance Liquid Chromatography HPLC Liquid Chromatography Mass Spectrometry LCMS Fragment Analyzer Capillary Electrophoresis<span><span><span><span><span><li> <li><span><span><span><span><span>Chromeleon Xcalibur ProSize 32 Karat<span><span><span><span><span><li> <li><span><span><span><span><span>Various analytical techniques such as UVVis spectroscopy Dynamic Light Scattering DLS osmometers platebased assays etc<span><span><span><span><span><li> <li><span><span><span><span><span>Biochemical techniques including quantitative Polymerase Chain Reaction qPCRDigital Droplet PCR ddPCR EnzymeLinked Immunosorbent Assay ELISA western blotting gelbased assays etc<span><span><span><span><span><li> <ul><li> <li><span><span><span><span><span>Demonstrated adaptability and comfort in dynamic work environments<span><span><span><span><span><li> <li><span><span><span><span><span>Meticulous attention to detail alongside proven problemsolving and organizational skills<span><span><span><span><span><li> <li><span><span><span><span><span>Excellent written and verbal communication skills<span><span><span><span><span><li> <li><span><span><span><span><span>Flexibility to work overtime when necessary as a prerequisite<span><span><span><span><span><li> <ul><p><span><span><span><b><span><span>Salary amp Benefits Offerings<span><span><b><span><span><span> <p><ul><li><span><span><span>Salary range is $65000 $90000year depending on experience<span><span><span><li> <li><span><span><span>Performance bonus amp Equity<span><span><span><li> <li><span><span><span>401k Match Program<span><span><span><li> <li><span><span><span>Healthcare Coverage<span><span><span><li> <li><span><span><span>Dental Coverage<span><span><span><li> <li><span><span><span>Vision Coverage<span><span><span><li> <li><span><span><span>Optional Dependent Care Account<span><span><span><li> <li><span><span><span>Flexible Spending Account FSA<span><span><span><li> <li><span><span><span>Paid Time Off PTO<span><span><span><li> <li><span><span><span>Company Paid Holidays<span><span><span><li> <li><span><span><span>Paid Sick Leave<span><span><span><li> <li><span><span><span>Onsite Fully Stocked Kitchens<span><span><span><li> <ul>
Lead Systems Analyst - Remote
Company: Prime Therapeutics
Location: Remote
Posted Mar 16, 2024
The text describes a job posting for a Lead Systems Analyst position at Prime Therapeutics LLC. The role involves managing work direction, leading and influencing team members, overseeing strategic initiatives, and creating logical designs based on architectural reviews. The ideal candidate should have a Bachelor's degree in Computer Science or related field, 5 years of experience in system requirements and business applications, and proven experience in leading others. Additional qualifications include excellent communication skills, strong analytical and problem-solving skills, and prior healthcare experience. The position offers a competitive salary range and benefits. The company is an Equal Opportunity Employer.
Director, Investor Relations & Corporate Communications (Hybrid)
Company: 4D Molecular Therapeutics - (4DMT)
Location: Other US Location
Posted Mar 16, 2024
<div> <p><em><strong>Attention recruitment agencies<strong> All agency inquiries are vetted through Talent Acquisition No unsolicited resumes will be accepted Agencies must be expressly engaged by the 4DMT talent acquisition team on any requisition Agencies reaching out directly to hiring managers will not be tolerated and may impact your ability to work with 4DMT in the future<em><p> <p><br ><p><p>4DMT is a clinicalstage biotherapeutics company harnessing the power of directed evolution for targeted genetic medicines We seek to unlock the full potential of gene therapy using our platform Therapeutic Vector Evolution TVE which combines the power of directed evolution with our approximately one billion synthetic AAV capsidderived sequences to invent evolved vectors for use in our products We believe key features of our targeted and evolved vectors will help us create targeted product candidates with improved therapeutic profiles These profiles will allow us to treat a broad range of large market diseases unlike most current genetic medicines that generally focus on rare or small market diseases <p> <p>We have built a deep portfolio of AVVbased gene therapy product candidates with five product candidates in clinical trials 4D150 for the treatment of wet agerelated macular degeneration wet AMD and diabetic macular edema DME 4D710 for the treatment of cystic fibrosis lung disease 4D310 for the treatment of Fabry disease cardiomyopathy 4D125 for the treatment of Xlinked retinitis pigmentosa XLRP and 4D110 for the treatment of choroideremia In addition we have two product candidates in preclinical studies 4D175 for geographic atrophy GA and 4D725 for alpha1 antitrypsin deficiency<p> <p>Todate we have demonstrated clinical proofofconcept for three evolved vectors in three therapeutic areas and routes of administration with five products and patient populations We believe this validates the power of our directed evolution platform for discovering superior vectors compared to wildtype viral vectors We have built a robust and efficient product engine with 6 open Investigational New Drug Applications INDs in the US 1 IND in Taiwan and 1 Clinical Trial Approval CTA in Australia We believe we are positioned to create develop manufacture and if approved effectively commercialize targeted genetic medicines that could transform the lives of patients suffering from debilitating diseases<p> <p>In addition to TVE our technology includes a robust AAV manufacturing platform and onsite manufacturing facility that allows us to rapidly produce and test research grade material and scale up to GMP clinical material This internal capability and close collaboration between our RampD and Manufacturing teams has greatly accelerated the pace of discovery at 4DMT<p> <p>Company Differentiators <p> <p> Fully integrated clinicalphase company with internal manufacturing<br > Demonstrated ability to move rapidly from idea to IND<br > Five candidate products in the clinic and two declared preclinical programs<br > Robust technology and IP foundation including our TVE and manufacturing platforms<br > Initial product safety and efficacy data substantiates the value of our platforms<br > Opportunities to expand to other indications and modalities within genetic medicine<p> <div> <p><u>GENERAL SUMMARY<u><p> <p>The Director Investor Relations amp Corporate Communications will work closely with the Head of Corporate Finance Investor Relations and Corporate Communications and the Chief Financial amp Business Officer to lead the planning management and execution of all investor relations and communications activities at the Company This role will be critical in furthering 4DMTs mission by conveying the Companys vision strategy values to both internal and external communities<p> <p>The successful candidate will possess a keen business sense and strategic vision a demonstrated track record of establishing relationships and credibility within the investment community and media and proven critical and strategic thinking while effectively utilizing data and analytics for decision making They will also have the ability to establish close working relationships with internal stakeholders and Competitive Intelligence team to craft actionable strategic insights amp establish communication strategy of internal priorities to the external community<p> <p>Experience in internal communications working closely with internal stakeholders is a plus<p> <p>This is a hybrid role requiring in office work 13 days a week as needed Bay Area candidates preferred<p> <p><u>RESPONSIBILITIES <u><p> <p><u>Investor Relations 40 of TIME<u><p> <ul><li>Develop integrate and execute comprehensive investor relations strategies that align with the Companys strategy<li> <li>Build and maintain strong relationships with current and potential investors provide analysts and investors with accurate and timely information about the Companys strategy<li> <li>Prepare executive team for investor events may be required to accompany executive team at events<li> <li>Manage and oversee an active investor relations calendar including the planning and execution of investor conferences nondeal roadshows and other banksponsored events companysponsored KOLRampD Day events and investor calls<li> <li>Draft press releases annual and quarterly reports earnings call scripts and corporate presentations<li> <li>Routinely track and analyze Company and competitive sellside analyst models and commentary with routine engagement and input from the finance team assess implications and make recommendations for communication and engagement<li> <li>Collaborate with senior crossfunctional leaders across the organization to share market intelligence and stakeholder perceptions of the Companys progress and performance ensure investors and other stakeholders are represented in the formation and execution of program and portfolio strategy and communications<li> <li>Manage external agencies and vendors that are supporting investor relations activities<li> <li>Aid our effort in building the next generation of genetic medicine leaders by being a key part to our learning organization<li> <ul><p><u>External Corporate Communications 40 of TIME<u><p> <ul><li>Develop integrate and execute comprehensive corporate communications strategies<li> <li>Lead a strategic communications plan that advances business goals and resonates with key audiences externally and internally<li> <li>Collaborate and coordinate with other functions internally to develop aligned and authentic messaging<li> <li>Serve as primary person to handle incoming inquiries from the media<li> <li>Continue to evolve the communications strategy to align with changes to the business<li> <li>In partnership with executive leadership team HR and PRIR firms manage and further develop our social media strategy and website<li> <li>Work closely with communications teams from external parties company community patient advocacy partnerships etc when coordinating joint PR and social media efforts<li> <li>Manage external agencies and vendors that are supporting corporate communications activities<li> <ul><p><u>Internal Corporate Communications 20 of TIME<u><p> <ul><li>Work closely with key internal stakeholders to develop effective employee communications plans that strengthen employee value proposition employee engagement recruitment and company culture<li> <li>Other duties as assigned nothing in this job description restricts managements right to assign or reassign duties and responsibilities to this job at any time<li> <ul><p><u>QUALIFICATIONS<u><p> <p><u>Education<u><p> <ul><li>Bachelors degree MBA or other advanced degree in a scientific area is preferred<li> <ul><p><u>Experience<u><p> <ul><li>10+ years of combined Investor Relations amp Corporate Communications experience in a rapidly growing emerging technologies life sciences firm<li> <li>5+ years in a leadership role managing a team<li> <ul><p><u>Skills<u><p> <ul><li>Investor Relations<li> <li>Expert in MS Power Point Word and Outlook<li> <li>Keen eye for creative design and refinement of publicfacing materials<li> <li>Strong presentation amp communication skills<li> <li>Ability to blend strategic and operational thinking<li> <li>Public amp media relations<li> <li>Social media<li> <ul><p><span datacontrast=auto>Base salary compensation range<span> <p> <p>Outside of Bay Area candidates range $180000yr $234000yr<p> <p>Bay Area based candidate range $215000yr $263000yr<p> <p>Please note the base salary compensation range and actual salary offered to the final candidate depends on various factors candidates geographical location relevant work experience skills and years of experience<p> <div> <p>4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race color religion gender sexual orientation national origin age disability genetic information marital status status as a covered veteran and any other category protected under applicable federal state provincial and local laws<p> <p> <p> <p>Equal Opportunity EmployerProtected VeteransIndividuals with Disabilities<p> <div>
Contract Senior Research Associate, Process Development
Company: Fate Therapeutics Inc
Location: San Diego, CA
Posted Mar 16, 2024
About Fate Therapeutics, Inc. For more information, please visit www.fatetherapeutics.com. Fate Therapeutics is headquartered in San Diego, CA. Equal Employment Opportunity Fate Therapeutics, Inc. is an equal opportunity employer. Strong attention to detail, analytical, time management, organizational and interpersonal skills. Using its proprietary iPSC product platform, the Company has established a leadership position in creating multiplexed-engineered iPSC lines and in the manufacture and clinical development of off-the-shelf, iPSC-derived cell products. / M.S. Will require working with hazardous materials. Occasional weekend work will be required. Privacy Notice To learn about how Fate collects and uses job application information, please visit Fate's online Privacy Notice.
Sr. Human Resources Generalist
Company: CymaBay Therapeutics
Location: North Jersey
Posted Mar 17, 2024
CymaBay is hiring for a Sr. Human Resources Generalist position. The role involves comprehensive HR support, including Talent Acquisition, Benefits, HRIS, Compliance, Employee Engagement, and Training. The position is hybrid, with work from home days on Monday and Friday, and in-office days on Tuesday, Wednesday, and Thursday. Essential duties include administrative support for Talent Acquisition, Onboarding, Benefits, Leaves of Absence, HRIS, Safety, Policy Management, Learning and Development, and Reporting. The ideal candidate should have a Bachelor's degree in HR or related field, 5+ years of generalist HR experience, strong knowledge of HR best practices and employment laws, excellent communication skills, and the ability to work independently. The anticipated salary range is $115,000 - $140,000.