Jobs at Click Therapeutics
249,921 open positions
Project Manager
Company: Apogee Therapeutics
Location: Remote
Posted Apr 13, 2024
Apogee Therapeutics is a well-funded biotechnology company seeking to develop differentiated biologics for the treatment of various inflammatory and immunology indications. The company offers a fast-paced, highly dynamic environment with opportunities for professional growth and development.
Data and Reporting Analyst - Remote
Company: Prime Therapeutics
Location: Remote
Posted Apr 15, 2024
The job posting is for a Data and Reporting Analyst position at Prime Therapeutics LLC. The role involves assessing, defining, and developing report deliverables, designing data repository and reporting tools, querying databases, compiling data, interpreting and analyzing data, and supporting staff training. The preferred qualifications include coding language experience, Excel experience, pharmacy experience, and Google Cloud Platform (GCP) experience. The potential pay range is from $52,250.00 to $78,390.00 based on experience and skills. Prime Therapeutics LLC is an Equal Opportunity Employer.
Associate Scientist, Bioanalytical
Company: Alloy Therapeutics, Inc.
Location: Waltham
Posted Apr 15, 2024
Alloy Therapeutics is a biotechnology company that empowers the global scientific community to develop better medicines. They offer pre-competitive tools, technologies, and services to all, with a focus on therapeutic biologics. The company is headquartered in Waltham, MA, with additional labs in the UK, Switzerland, and Georgia. They have 82VS portfolio companies across Boston, San Francisco, Dallas, and Oklahoma City. Alloy values accountability, trust, and open communication, and they reinvest 100% of their revenue in innovation and access to innovation. They are currently seeking an Associate Scientist to join their Global Bioanalytics group, supporting the discovery of antibody-based therapeutics. The role involves biochemical and biophysical characterization of antibodies, data analysis, and collaboration within a cross-functional scientific environment.
Director of Toxicology
Company: BlueRock Therapeutics
Location: Cambridge
Posted Apr 17, 2024
<div><u><b>Who is BlueRock<b><u><div> <p><br ><p> <p><span>BlueRock Therapeutics a whollyowned and independently operated subsidiary of Bayer AG is a leading engineered cell therapy company using its unique <span><b><i>cell+gene<i><b><span> platform to direct cellular differentiation and genetically engineer cells to create a new generation of cellular medicines that address large patient populations suffering from neurological cardiovascular and immunology diseases<span><p> <p><span>The convergence of cell biology and genetic engineering is creating fundamental new ways to impact disease Founded in 2016 to capitalize on these technological breakthroughs we are advancing our novel <span><b><i>cell+gene<i><b><span> platform to develop manufacture and deliver an entirely new generation of authentic and engineered cell therapies across three therapeutic areas neurology cardiology and immunology<span><p> <p><br ><p> <div><u><b>What Are We Doing<b><u><div> <p><br ><p> <p><span>Our foundational science harnesses the ability to create and then direct the differentiation of universal pluripotent stem cells into authentic functional cells that can be used as allogeneic cellular therapies to treat a broad array of diseases We can also further engineer these cells enabling them to produce enzymes antibodies and other proteins for additional therapeutic benefit <span><p> <p><span>We are passionate about delivering on the promise of cellular and gene therapy shaping the future of cellular medicine and delivering new therapies to millions of patients with treatment options <span><p> <p><span>We are seeking individuals who are collaborative thrive in a fun and dynamic culture and are steadfast in the commitment to advance cuttingedge cellular therapies to impact patients lives<span><p> <p><br ><p> <p><span>Director of Toxicology leads nonclinical safety within Preclinical Development and is responsible for coordinating nonclinical safety to adequately support BlueRock programs from research through development stages Working across numerous functional groups and testing facilities the position is accountable for all phases of nonclinical safety of human induced pluripotent stem cell hiPSCderived authentic cells prior to initiating clinical trials Director of Toxicology assures adequate strategy for nonclinical INDenabling studies in conjunction with program teams to support clinical testing and provides input as a technical expert within the immediate function and within a multidisciplinary project team <span><p> <p><br ><p> <p><span>This dynamic position works closely with program team members across various functional groups within BlueRock assures nonclinical development studies both GLP and nonGLP are performed according to the study protocol at external CROs and compiles nonclinical documents for regulatory submissions An ideal employee will be passionate to contribute to advance programs and to deliver safe cell therapies to patients<span><p> <p><b>Responsibilities<b> <p><ul><li>Lead nonclinical safety within Preclinical Development <li> <li>A nonclinical development representative of project teams throughout various program stages of the life cycle <li> <li>Support and advise Research in nonclinical safety evaluation of earlystage programs identify deficiencies and aid to fill data gaps to advance programs to development <li> <li>Interact crossfunctionally with key stakeholders to advance the program based on the nonclinical development strategy <li> <li>Work closely with Toxicology Operations on vendor qualification study setup protocol development study monitoring data and report review and maintain timeline and study budget for each study<li> <li>Ensure GLP compliance and appropriateness of nonclinical model welfare at CROs <li> <li>Act as a Sponsor Representative on nonclinical studies performed at CROs and maintain active communication line with the CRO <li> <li>Align study designs and dose setting within Preclinical Development and Project Team <li> <li>Independently ensures the preparation of technical documents including position papers risk assessments and safety summaries <li> <li>Compile nonclinical portion of regulatory submission documents eg INDCTA regulatory interactions <li> <li>Interaction with regulatory agencies as needed<li> <li>Communicate with clinical team on the clinical development plan review clinical protocol compilation of Investigators Brochure and provide input to Target Product Profile <li> <li>Collaborate on externally partnered programs as necessary <li> <li>Perform program due diligence as assigned <li> <li>Coordinate with consultants as needed <li> <li>Provide written and oral presentations internally and externally as required<li> <li>Participate in project sub teams or departmental working groups<li> <ul><p><b>Minimum Requirements<b> <p><ul><li>PhD or a degree commensurate with experience <li> <li>American Board of Toxicology ABT certification is a plus <li> <li>A minimum of six 6 years of toxicology experience in pharmaceutical industry <li> <li>A broad knowledge of research and development process <li> <li>Experience in cell andor gene therapy modality is a plus<li> <li>Familiarity of regulatory guidance eg ICH FDA EMA and experience in GLP studies<li> <li>A proven track record of successful IND compilation<li> <li>Exposure to working in a projectprogram team environment<li> <li>Excellent oral and written communication <li> <li>Able to travel up to 10<li> <ul><p> <p><p>LIAL1<p> <p><br ><p> <p><b>BlueRock Therapeutics Company Culture Highlights<b><p> <p>Winner of Boston Business Journals Best Places to Work Midsize Company 2023<p> <p>Winner of Comparablys Award for Best Company for Diversity 2022<p> <p>Winner of Comparablys Award for Best Company for Women 2022<p> <p>Winner of Comparablys Award for Best CEO 2022<p> <p>BlueRock Therapeutics is ranked in the top 5 of companies for Overall Culture on Comparably<p> <p>Engineering Department is ranked in the top 5 of companies for Overall Culture on Comparably<p> <p><br ><p> <p>Check us out on Comparably httpswwwcomparablycomcompaniesbluerocktherapeutics<p> <p>Follow us on Linkedin httpswwwlinkedincomcompanybluerocktx<p> <p><br ><p> <div><u><b>Equal Opportunity Workplace<b><u><b> <b><i>At BlueRock we welcome and support differences and diversity and we are proud to be an equal opportunity workplace Please let us know if you require disabilityrelated accommodation or other grounds protected by human rights legislation during the recruitment process so that we can work with you to meet your needs<i><div> <p><p>
Sr Manager, Statistics
Company: Corcept Therapeutics
Location: Peninsula
Posted Apr 13, 2024
Corcept is a leading company in the research and development of cortisol modulators, with over 1,000 proprietary molecules discovered. They received FDA approval for Korlym® (mifepristone) in 2012, the first treatment for hypercortisolism (Cushing syndrome). Currently, they have more than 30 ongoing studies across various disease areas, including endocrinology, oncology, metabolism, and neurology. The Sr Manager, Statistics will lead the statistical components of Corcept's clinical studies, partnering with various teams and ensuring regulatory compliance. The role requires a PhD in Statistics, Biostatistics, or Mathematics, and at least 5 years of experience in clinical trials and the pharmaceutical industry.
Senior Content Designer
Company: Click Therapeutics
Location: Raleigh-Durham, NC
Posted Apr 12, 2024
Click Therapeutics is a leading innovator of Digital Therapeutics, developing software as prescription medical treatments for people with unmet medical needs. They are looking for a Senior Content Designer to develop the voice, content strategy, and content for their patient-facing digital therapeutic applications.
Senior Director National Accounts
Company: BioXcel Therapeutics
Location: Remote
Posted Apr 17, 2024
<p>The Sr Director National Accounts is responsible for negotiating coverage reimbursement for designated products within assigned account areas through contracting where necessary and noncontracting opportunities where possible The incumbent assesses and diagnoses the current business environment in each key account to gain positive formulary access for the company portfolio with minimal restrictions Account responsibilities include but are not limited to Pharmacy Benefit Managers NationalRegional Health Plans State Medicaid Medicaid PBMS ie Change Healthcare Magellan etc and major SPs and LTC providers<p> <p><b>AccountabilitiesThe Primary Responsibilities of this role include but are not limited to<b> <p><ul><li>Facilitates account management by assessing contracting options coordinating selling activities and customer interactions through effective leadership communication and implementation with CADs to ensure appropriate customer needs are metexceeded<li> <li> Develops and implements partnerships with cross functional counterparts to build a successful comprehensive business plan to gain product trial and adoption This includes but is not limited to comprehensive account profile business strategies financial models key result areas information systems inventory management strategies competitive intelligence for each account current resources being utilized execution of above follow up action steps to ensure compliance and coordinationprocurement of available resources etc<li> <li>Develops establishes and strengthens successful business partnerships with external partners and stakeholders including but not limited to executive management Chief Executive Officer CEO Chief Financial Officer CFO Director of Pharmacy Services Contracting Directors Director of industry relations State Medicaid officials and fiscal intermediaries etc medical directors key physicians and secondary customers ie pharmacists nurses and other health care professionals<li> <li>Implements approved plans and monitors plan execution against high priority accounts<li> <li>Develops and implements business reviews of key accountsmarketplace on an agreed upon consistent basis with the VP Market Access<li> <li>Serves as a subject matter expert SME and resource in collaboration with CADs when appropriate for accounts within their areas<li> <li>Executes customer calls consultations on regional accounts outside of assigned key accounts and specific skill building initiatives with CADs on managed care selling to drive formulary pull through<li> <li>Participates in key conventions as needed ie Academy of Managed Care Pharmacy AMCP National Association of Managed Care Physicians NAMCP Pharmaceutical Care Management Association PCMA Asembia etc<li> <li>Convey appropriate and professional image to external customers that is aligned to BioXcel core values<li> <li>Strictly adhere to BioXcel code of conduct guidelines TE policy and other policies as written as well as ensuring IS reps comply<li> <li>Assist as needed in projects that drive BioXcel towards the mission of being the Preeminent CNS biopharmaceutical company in 5 years<li> <ul><p><b>Required Education Skills and Experience<b> <p><ul><li>Bachelors degree in the health sciences businessmarketing or related field Masters Degree preferred<li> <li>A minimum of 15 years relevant pharmabiotech industry experience in a variety of roles market access national account director payer marketing sales leadership and marketing Strategic responsibility OR a combination of education and relevant experiences in the pharmabiotech industry in positions of increasing technical and strategic responsibility<li> <li>Strong understanding of the US payer environment payer market dynamics payer marketing principles and market access organization decision making process<li> <li>Proven track record of building strong relationships with key decision makers<li> <li>Proven record of high ethical values and health care compliance<li> <li>Demonstrated ability to work closely with CADs on account pull through and local training<li> <li>Demonstrated ability to access analyze and present data<li> <li>PBM and pull thru experience post signed contract<li> <li>National Account management experience with a successful track record within target accounts<li> <ul><p><b>Desirable Education Skills and Experience<b> <p><ul><li>Leading a national payer account team<li> <li>CNS launch experience<li> <li>Proven track record of successful pharmabiotech sales and sales management experience in the CNS space calling on psychiatrists and neurologists<li> <li>Experience successfully contracting and negotiating with Managed Care Organizations MCOs Pharmacy Benefit Managers PBMs State Medicaid decision makersPBMs ie Change Healthcare Magellan Integrated Delivery Networks IDNs and Health Systems<li> <li>Experience in CNS therapeutic area<li> <li>Experience in a combination of large and startup companies<li> <ul><p><b>Competencies<b> <p><ul><li>Strategic Thinking and Execution Utilizes all resources to prioritize plan and make good decisions regarding time allocation to drive business results Regularly updates and adjusts business plans strategies and acts with urgency<li> <li>Patient Focused Clinical Acumen Builds and maintains a deep understanding of relevant patient types treatment options and patient flow within the ecosystems relevant to promoted products<li> <li>Influence and Impact Communicates authentically thoughtfully and persuasively via BioXcel Principles Conveys a professional positive and enthusiastic presence in all verbal and written communication<li> <li>Personal Leadership Embraces a growth mindset and operates with grit in a fast paced startup environment adapting readily to change Is selfdirected pursues excellence and holds selfaccountable to timelines and commitments<li> <li>Teamwork and Collaboration Seeks the input of others to determine the best course of action Proactively shares ideas and best practices with colleagues across the organization specifically in alignment of cross functional colleagues collaboration efforts<li> <li>Market Expertise High capacity to understand the health care business specific to the role<li> <li>Planning and Organizing Able to manage the administrative aspects of the role Proficient with Microsoft Word Excel PowerPoint etc<li> <ul><p><b>BioXcel Value Drivers<b> <p><ul><li>Patient Focused is the mindset in all that we do so that our patients and their families are impacted in ways that are meaningful and valuable<li> <li>Integrityopen and honest communication with uncompromising principles and ownership<li> <li>Collaborativethis is how we work together towards shared goals in a synergistic environment that fosters innovative ideas and approaches<li> <li>Agilewillingness and ability to move quickly and adjust to everchanging business needs to achieve goals<li> <ul><p><b>Required<b> <p><ul><li>Align to the culture and Value Drivers of BioXcel Therapeutics<li> <li>Matching skill set and beliefs to the key competencies listed above<li> <li>Excellent written and oral communication and presentation skills<li> <li>ProvenDocumented sales success and national account objectives success<li> <li>Strong Planning and organization skills<li> <li>Previous use and knowledge of CRM<li> <li>Remote position Daily and overnight travel weekly of up to 50 proximity to major airport desirable<li> <ul><p> <p><p><i><b>Your Path to Endless Opportunities<b><i><p> <p><br ><p> <p>If youre looking to push the envelope and join an innovative company where technology meets drug discovery and development and youre enthusiastic creative with a passion for cuttingedge research you should join our team We are looking for highly motivated passionate employees to help us drive technology solutions for discovering breakthrough treatments for our portfolio of oncology and neuroscience programs as well as for our partners across major therapeutic areas<p> <p><br ><p> <p><b>About BioXcel Therapeutics Inc<b><p> <p><br ><p> <p>BioXcel Therapeutics Inc is a commercialstage biopharmaceutical company utilizing artificial intelligence approaches to develop transformative medicines in neuroscience and immunooncology The Companys drug reinnovation approach leverages existing approved drugs andor clinically validated product candidates together with big data and proprietary machine learning algorithms to identify new therapeutic indices The Companys commercial product IGALMI™ developed as BXCL501 is a proprietary sublingual film formulation of dexmedetomidine approved by the FDA for the acute treatment of agitation associated with schizophrenia or bipolar I or II disorder in adults The safety and effectiveness of IGALMI has not been established beyond 24 hours from the first dose BXCL501 is also being evaluated for the acute treatment of agitation associated with Alzheimers disease and as an adjunctive treatment for major depressive disorder The Company is also developing BXCL502 as a potential therapy for chronic agitation in dementia and under its subsidiary OnkosXcel Therapeutics BXCL701 an investigational orally administered systemic innate immunity activator for the treatment of aggressive forms of prostate cancer and advanced solid tumors that are refractory or treatment naïve to checkpoint inhibitors For more information please visit wwwbioxceltherapeuticscom <p> <p><br ><p> <p><span>EOEMFVSO<span><p> <p><span>BioXcel Therapeutics is an Equal Opportunity Employer All qualified candidates will receive consideration for employment without regard to race color religion sex national origin disability gender identity sexual orientation or protected veteran status<span><p> <p><p>
Senior Manager, Competitive Intelligence
Company: 4D Molecular Therapeutics - (4DMT)
Location: Other US Location
Posted Apr 13, 2024
4DMT is a clinical-stage biotherapeutics company specializing in gene therapy. They have a robust platform, Therapeutic Vector Evolution (TVE), which combines directed evolution with synthetic AAV capsid-derived sequences to create evolved vectors for their products. The company has five product candidates in clinical trials and two in preclinical studies, targeting a broad range of large market diseases. 4DMT's technology includes a robust AAV manufacturing platform and onsite manufacturing facility, enabling rapid production and testing of research grade material. The company is positioned to create, develop, manufacture, and commercialize targeted genetic medicines. The Senior Manager of Competitive Intelligence is a key role, responsible for leading and managing primary and secondary competitive intelligence activities, supporting strategy analyses, and communicating with key stakeholders.
Senior Software Prototype Engineer
Company: Click Therapeutics
Location: Raleigh-Durham, NC
Posted Apr 12, 2024
Click Therapeutics is a leading innovator in Digital Therapeutics, developing and commercializing software as prescription medical treatments for various unmet medical needs. The company focuses on psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. They are seeking a prototyping software engineer to collaborate with science, product, and clinical operations teams to develop full-stack, cross-platform mobile applications for exploratory research and clinical studies. The ideal candidate should have 8+ years of full-stack software development experience, comfort with ambiguity, and a pioneering attitude. The role offers a competitive salary, annual performance-based cash bonus, and a generous equity package, along with comprehensive benefits and a flexible work arrangement.
Senior Software Engineer
Company: Click Therapeutics
Location: Raleigh-Durham, NC
Posted Apr 12, 2024
Click Therapeutics, a leading innovator in Digital Therapeutics, is seeking an experienced software engineer to expand their platform. The role involves developing and maintaining software for existing and new therapeutic applications, focusing on a unified user experience. The engineer will work closely with a collaborative team, participating in code reviews, brainstorming sessions, and product requirement planning. The position offers a competitive salary, performance-based bonuses, and a generous equity package. The company is committed to equal opportunity and offers a comprehensive benefits package, including unlimited PTO, professional development stipends, and more. The role can be based in Tribeca, NYC or Raleigh, NC, with a hybrid working model.
Senior Product Manager
Company: Click Therapeutics
Location: Raleigh-Durham, NC
Posted Apr 12, 2024
Click Therapeutics is seeking a Senior Product Manager to collaborate with various experts and deliver pipeline products through clinical trials and to market. The role involves working in an Agile environment, understanding scientific concepts, and translating them into testable products. The company offers a competitive salary, benefits, and a generous equity package. The position can be based in Tribeca, NYC or Raleigh, NC with a hybrid working model.
SVP, Head of Data Analytics
Company: Dyne Therapeutics
Location: Waltham
Posted Apr 17, 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>The Senior Vice President SVP Head of Data Analytics leads a multidisciplinary team responsible for biostatistics statistical programming and data management This strategic leadership position requires a broad knowledge of clinical data management programming and statistical analysis tools to plan studies and interpret results from clinical modelling and simulation and epidemiologic studies We are seeking a visionary leader with deep expertise in data analytics a proven track record of driving innovation and a passion for advancing rare disease research We are committed to leveraging cuttingedge science and innovative technologies to accelerate drug discovery and improve patient outcomes This role plays a pivotal role in driving datadriven decisionmaking across all stages of drug development<p> <p>The SVP Head of Data Analytics is a subject matter expert concerning global regulatory agencies as well as ICH guidelines and regulations applicable for the conduct analysis and reporting of clinical trials in rare diseases This person provides coaching to team members to enable them to engage in and provide quality input at internal and external meetings including regulatory interactions and meetings with key opinion leaders This person is a strong advocate within Dyne for Data Analytics involvement taking a prominent role in research amp development<p> <p><strong>Primary Responsibilities include<strong><p> <ul><li>Provide strategic direction and leadership for the data analytics function aligning with corporate goals and objectives<li> <li>Establish and execute on a strategic roadmap for biostatistics statistical programming and data management for Dyne as we prepare for commercialization<li> <li>Serve as the subject matter expert and point person for data analytics for interactions with regulatory agencies bringing in team members as appropriate<li> <li>Develop and implement a comprehensive data analytics strategy to support the companys rare muscle disease pipeline<li> <li>Lead and mentor a highperforming team of biostatisticians statistical programmers and clinical data managers<li> <li>Foster a culture of collaboration innovation and continuous learning to drive team success<li> <li>Provide organizational leadership to balance time quality and cost requirements<li> <li>Strategically set people goals including internal career development and talent management as well as alternative resourcing strategies where needed<li> <li>Establish robust data governance processes and standards to ensure the quality integrity and security of clinical trial data<li> <li>Implement best practices for data collection management and analysis in compliance with regulatory requirements<li> <li>Oversee the design and execution of statistical analysis plans for clinical trials including sample size calculations randomization schemes and statistical modeling<li> <li>Provide strategic input on study design endpoints and statistical methodologies<li> <li>Direct the development and validation of statistical programming code for the analysis and reporting of clinical trial data<li> <li>Ensure adherence to programming standards best practices and global regulatory guidelines<li> <li>Lead the clinical data management team in the collection cleaning and validation of clinical trial data<li> <li>Implement data management processes and systems to support efficient and accurate data capture and analysis<li> <li>Collaborate closely with crossfunctional teams including clinical development regulatory affairs and medical affairs to support datadriven decisionmaking<li> <li>Communicate key findings insights and recommendations to senior leadership and external stakeholders<li> <li>Be accountable for timely production and accuracy of all statistical analyses and integrated scientific reports for clinical trial results publications activities scientific presentation and regulatory submissions both local and international<li> <ul><p><strong>Education and Skills Requirements<strong><p> <ul><li>PhD or MS in Biostatistics Statistics Epidemiology or related field Certification in clinical data management eg CDM certification is a plus<li> <li>Minimum of 20 years of progressive experience in data analytics biostatistics or clinical data management within the pharmaceutical or biotechnology industry including managerial expertise<li> <li>Prior experience in rare disease drug development is highly desirable<li> <li>Demonstrated track record of strategic leadership team management and organizational development Proven ability to inspire and motivate teams to achieve excellence<li> <li>Expertise in statistical analysis methodologies including clinical trial design survival analysis longitudinal data analysis and Bayesian methods<li> <li>Proficiency in statistical programming languages eg SAS R and clinical data management systems eg Medidata Rave Oracle Clinical is essential<li> <li>Indepth understanding of regulatory requirements and guidelines related to clinical trial design data collection and analysis eg FDA EMA ICH<li> <li>Excellent written and verbal communication skills with the ability to effectively communicate complex scientific concepts to diverse audiences<li> <li>Strong interpersonal skills and the ability to collaborate effectively with crossfunctional teams in a matrixed environment<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>