Jobs at Click Therapeutics
249,921 open positions
Digital Account Manager
Company: Click Here Digital
Location: Baton Rouge, LA
Posted Sep 16, 2023
)Strong understanding of SEM, SEO, Online Display, and Social Media marketingExperience in selling digital marketing solutionsBachelor's degree in Advertising, Business, or Communications or equivalent experience Job Responsibilities: Plan and execute digital marketing strategies based on client goals and objectives, and consult with clients on processes and industry best practicesDaily client communication on advertising strategy and campaign performanceMonitor and analyze the effectiveness of marketing strategies and translate data from campaign performance results into an actionable narrative for clients.Travel for client consultations monthly.Coordinate cross-functional teams to ensure the success of campaign delivery, performance, and executionOther duties may be assigned Required Qualifications: Experience working in client services, sales, marketing, and/or advertisingKnowledge of the automotive sales industry and processesExceptional communication skills, both verbal and written, with the ability to convey complex technical information in a concise manner to clients across all levels of organizationsAbility to analyze data sets and identify trends based on industry KPIsConfident in building and maintaining strong client relationshipsExcellent time-management and organizational skillsExperience using industry tools (Google Analytics, Google Search Console, Google Adwords, Facebook Business Manager, etc. Candidates that excel at relationship building, analyzing data, and are self-motivated will thrive in this role. These channels include Search Engine Marketing (PPC), Programmatic Display and Video, Connected TV (OTT and CTV), Search Engine Optimization (SEO), Social Media Marketing, and Website Development. This position is dedicated to focusing on client satisfaction. The Account Manager will be responsible for providing exceptional support to our clients and partners and assisting in ways to drive revenue growth while identifying new opportunities. At Click Here Digital, our Account Managers work directly with dealership executives across the United States to create integrated digital marketing strategies that utilize multiple channels to provide clients with the best return on investment.
Analyst I, QC Microbiology (Contract)
Company: Allogene Therapeutics
Location: East Bay
Posted Sep 18, 2023
Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law.As an equal opportunity employer, Allogene is committed to a diverse workforce. This position provides Quality Control microbiological testing for clinical and commercial manufactured product, responsible for product testing, utility testing and environmental monitoring. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients. This is a 6+ month contract opportunity in Newark, CA.Responsibilities include, but are not limited to:Perform environmental monitoring of utilities and facilities and manage test data in LIMSPerform Endotoxin and Sterility testing of final drug product per compendial methodsPerform media growth promotion, gram staining, and microbial ID test methods of isolates per compendial methodsPerform TOC testing of water samplesPerform bioburden and Endotoxin testing of incoming raw materialsWork with internal and external resources to maintain lab in an optimal stateMonitor and trend dataAssemble reports on findings from environmental monitoring of Allogene’s cGMP facility, frequently update management on environmental trends and implement corrective action plans when necessary Revise and review SOPsAssist in investigations regarding out of specifications (OOS) results and toaddress deviations related to microbiological procedures.Follow GMP processes to ensure compliance with documented policiesGather metric information for use in continuous improvement of areas of responsibilityPerform other duties as requiredPosition Requirements & Experience:Bachelor’s degree in Microbiology preferred or equivalent experience Experience in a QC Microbiology laboratory settingExperience in the application of microbiological techniques such as air monitoring gases, water testing, surface monitoring.Experience in sterile gowning procedures, aseptic techniques and clean room operations is a plusKnowledge of GMP, SOPs and quality control processesExperience with LIMS (i.e. MODA) and Sievers M9s for TOC testing is a plusProficient in MS Word, Excel, Power Point and other applications.Excellent interpersonal, verbal and written communication skills are in this collaborative work environment.Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities.Excellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelines.Ability to work independently and as part of a team.Strong interpersonal skills including verbal and written communication are essential in this collaborative work environment.Candidates must be authorized to work in the U.S.We offer a chance to work with talented people in a collaborative environment. For more information, please visit www.allogene.com, and follow @AllogeneTx on Twitter and LinkedIn.About the role:Allogene is seeking a highly motivated individual to join us as an Analyst I, QC Microbiology. Led by world-class management with significant experience in cell therapy, our fully integrated, in-house team of researchers is dedicated to discovery and translational research, development, and cell manufacturing.At Allogene, we are developing a pipeline of off-the-shelf CAR T cell candidates, with the goal of delivering readily available cell therapy faster, more reliably, and at greater scale to more patients. The expected salary range for this role is $28.00 to $32.00 per hour. About Allogene:Allogene Therapeutics is a clinical-stage biotechnology company with a single-minded focus on pioneering the development of investigational allogeneic chimeric antigen receptor T cell (AlloCAR T™) products for cancer.
Scientist/Scientist II, Research Technologies
Company: Shape Therapeutics
Location: Boston, MA
Posted Sep 16, 2023
Employees are eligible to enroll in our Company’s voluntary 401k plan, voluntary Life/AD&D and Voluntary FSA’s.The salary range for the Scientist/Scientist II role is $96,000-$144,000. Meet some of the team members here.What You’ll Do: Assay Optimization: Work collaboratively with our Automation Engineer to optimize cell and molecular biology assays for automation, ensuring accuracy and reliability. Workflow Integration: Collaborate closely with the Automation Engineer to integrate optimized assays into automated workflows, streamlining laboratory processes.Data Analysis: Analyze and interpret data generated from automated experiments, identifying areas for improvement and refinement, and make data-driven decisions.Problem Solving: the ability to quickly diagnose problems, identify solutions, and maintain a can-do attitude.Documentation: Maintain comprehensive documentation of assay protocols, automation processes, and troubleshooting procedures.Collaborative Research: Collaborate with cross-functional teams of scientists to contribute to cutting-edge research projects.Continuous Improvement: Stay updated on the latest advancements in cell and molecular biology and automation technologies, recommending and implementing improvements to assays and processes.Quality Assurance: Implement quality control measures to ensure the accuracy and reliability of automated assays. What You Bring: Cell and Molecular Biology Expertise: A strong background in cell and molecular biology, with hands-on experience in assay development, cell culture, molecular techniques, and NGS. Automation: Experience and familiarity with automation systems and the ability to collaborate effectively with an Automation Engineer to integrate assays into automated workflows. Collaboration: Proven ability to work collaboratively in cross-functional teams, particularly with Automation Engineers, to optimize and automate laboratory processes.Detail-Oriented: Meticulous attention to detail and a commitment to producing high-quality, reproducible results.Analytical Skills: Proficiency in data analysis and interpretation, with the ability to troubleshoot and refine assays for improved performance.Problem-Solving: Strong problem-solving skills and the ability to adapt assays to meet specific research needs.Communication Skills: Excellent communication skills, both written and verbal, to document experimental procedures and collaborate effectively with team members.Innovation: A passion for innovation and a desire to push the boundaries of scientific research through automation.Education & Experience: A PhD in Biology or a related discipline. We are proud to offer a competitive paid parental leave benefit, an annual employee stipend for employees to use however they choose, a Flex Paid Time Off program (allowing flexible PTO for vacation, sick leave, and other purposes) and Company paid Long Term Disability. Thriving in a fast-paced startup environment, characterized by autonomy, initiative, and a shared passion for research, along with excellent communication and collaboration is essential to excel in this role. Non-PhD candidates with 5-10+ years of at-the-bench experience and demonstrated success within the biotech industry will be considered. ShapeTX offers a robust benefits package, including but not limited to: Medical, Dental and Vision coverage for employees and their eligible dependents. not only through our science, but also through our commitment to foster an inclusive environment that supports diverse perspectives and experiences. Additional compensation may include annual target bonus and/or sign-on bonus, equity grant and relocation bonus.We aspire to Shape Life! Additionally, maintaining a can-do attitude even in the face of technical challenges will be a valuable asset to our team's success. You will join our satellite site in Boston. The hired applicant's placement within the range is based on qualifications and professional experience. You can find us at shapetx.com and on LinkedIn and Twitter.At ShapeTX, we are a dynamic team of professionals who are dedicated and passionate about making cures a reality.
Supervisor, IT Operations
Company: CymaBay Therapeutics
Location: North Jersey
Posted Sep 19, 2023
)Demonstrate a “can-do” approach to problem solving and conflict resolutionWilling and able to both lead and be hands-onFlexibility and adaptability in adjusting to changing priorities and requirements in a rapidly growing organizationIn-depth knowledge of Microsoft Azure, Microsoft Windows OS’s (10, 2016, 2019), JAMF/Mac OS Management, Intune MDM, Network Hardware /Security (including DNS, firewalls, and VPN), power (including UPS)Expert knowledge of Salesforce/Veeva, OKTA, Office365, Code42 Crashplan, Zoom, Box, etc.The anticipated salary range in Newark, California is $145,000-$155,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Implement security solutions, cloud backup, identity management and monitoring/reporting solutionsCreate runbooks and knowledge articles in order to resolve frequently occurring issues.Act as an escalation point for the resolution of technical requests - ensuring both accuracy and timely closure of issuesProvide exceptional service delivery to all customers, including executives, internal and external team membersCoordinate IT Operations deliverables with internal IT members and external vendorsDevelop and maintain IT policies and procedures to ensure compliance with industry regulations and best practices in the areas of network/network security, disaster recovery, service monitoring, etc.Manage service outages and provide timely communication to business stakeholders.Ensure system governance is maintainedLead IT change control efforts within the organizationContinually assess technologies, vendors, and services to ensure operational excellenceStay current in technology specific to technical operations, infrastructure monitoring, risk management, security, IT best practices, and regulatory requirementsAs stakeholder of IT infrastructure, ensure corporate SOP’s are followed with particular attention to systems under SOX and GxP controlsPerform other responsibilities as assignedMINIMUM QUALIFICATIONSMinimum of 5-7 years of experience in an IT function, preferably in a Biopharma/Life Sciences industryBachelor’s degree in Information Technology, or related fieldExcellent written and oral communication skillsExceptional analytical, conceptual, and problem-solving abilitiesOperate with a sense of urgency and focusKnowledge and understanding of relevant legal and regulatory requirements (SOX, GxP, etc. CymaBay is a multi-state employer, and this salary range may not reflect positions that work outside of the Bay Area or in other states. As a team member delivering technical services, this individual will partner with Business Applications team and Service Desk Lead. This role requires extensive knowledge in enterprise infrastructure services along with working knowledge of business systems commonly utilized in emerging Life Sciences organizations. This role is located in Newark, CA and is required to be onsite 5 days a week.ESSENTIAL DUTIES AND RESPONSIBILITIESManage and supervise the delivery of IT infrastructure and technical operationsProactively manage and implement IT systems and infrastructure in support of organizational needs and technical challengesMonitoring the performance and security of IT systems and infrastructure, identifying, and addressing any issues or problems that ariseManage and execute the delivery of service in alignment to IT roadmapStay hyper focused on the security and integrity of the organization's IT systems and data. POSITION SUMMARYReporting to the Head of Information Technology (IT), this position will be responsible to lead, plan, coordinate, and administer solutions focused on the delivery of IT infrastructure and cloud native business technologies.
Supervisor, IT Operations
Company: CymaBay Therapeutics
Location: North Jersey
Posted Sep 19, 2023
)Demonstrate a “can-do” approach to problem solving and conflict resolutionWilling and able to both lead and be hands-onFlexibility and adaptability in adjusting to changing priorities and requirements in a rapidly growing organizationIn-depth knowledge of Microsoft Azure, Microsoft Windows OS’s (10, 2016, 2019), JAMF/Mac OS Management, Intune MDM, Network Hardware /Security (including DNS, firewalls, and VPN), power (including UPS)Expert knowledge of Salesforce/Veeva, OKTA, Office365, Code42 Crashplan, Zoom, Box, etc.The anticipated salary range in Newark, California is $125,000-$135,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Implement security solutions, cloud backup, identity management and monitoring/reporting solutionsCreate runbooks and knowledge articles in order to resolve frequently occurring issues.Act as an escalation point for the resolution of technical requests - ensuring both accuracy and timely closure of issuesProvide exceptional service delivery to all customers, including executives, internal and external team membersCoordinate IT Operations deliverables with internal IT members and external vendorsDevelop and maintain IT policies and procedures to ensure compliance with industry regulations and best practices in the areas of network/network security, disaster recovery, service monitoring, etc.Manage service outages and provide timely communication to business stakeholders.Ensure system governance is maintainedLead IT change control efforts within the organizationContinually assess technologies, vendors, and services to ensure operational excellenceStay current in technology specific to technical operations, infrastructure monitoring, risk management, security, IT best practices, and regulatory requirementsAs stakeholder of IT infrastructure, ensure corporate SOP’s are followed with particular attention to systems under SOX and GxP controlsPerform other responsibilities as assignedMINIMUM QUALIFICATIONSMinimum of 5-7 years of experience in an IT function, preferably in a Biopharma/Life Sciences industryBachelor’s degree in Information Technology, or related fieldExcellent written and oral communication skillsExceptional analytical, conceptual, and problem-solving abilitiesOperate with a sense of urgency and focusKnowledge and understanding of relevant legal and regulatory requirements (SOX, GxP, etc. CymaBay is a multi-state employer, and this salary range may not reflect positions that work outside of the Bay Area or in other states. As a team member delivering technical services, this individual will partner with Business Applications team and Service Desk Lead. This role requires extensive knowledge in enterprise infrastructure services along with working knowledge of business systems commonly utilized in emerging Life Sciences organizations. ESSENTIAL DUTIES AND RESPONSIBILITIESManage and supervise the delivery of IT infrastructure and technical operationsProactively manage and implement IT systems and infrastructure in support of organizational needs and technical challengesMonitoring the performance and security of IT systems and infrastructure, identifying, and addressing any issues or problems that ariseManage and execute the delivery of service in alignment to IT roadmapStay hyper focused on the security and integrity of the organization's IT systems and data. POSITION SUMMARYReporting to the Head of Information Technology (IT), this position will be responsible to lead, plan, coordinate, and administer solutions focused on the delivery of IT infrastructure and cloud native business technologies.
Automation Engineer
Company: Shape Therapeutics
Location: Boston, MA
Posted Sep 19, 2023
Employees are eligible to enroll in our Company’s voluntary 401k plan, voluntary Life/AD&D and Voluntary FSA’s.The salary range for the Automation Engineer role is $120,000-$200,000. Meet some of the team members here.What You’ll Do: Biotech/Pharmaceutical Experience: Proven experience in building automated pipelines for research and development within the biotech or pharmaceutical industry. Automation Expertise: Proficiency in designing and building automated workflows for RNA and DNA extractions, cellular assays, and NGS (Next-Generation Sequencing) sample preparation. End-to-End Vision: Ability to conceptualize and construct end-to-end automated workflows, optimizing efficiency and accuracy in laboratory processes. Data Management: Familiarity with data storage systems to effectively track and manage data generated from automated experiments. Autonomous: Self-driven and able to work independently with minimal supervision, taking initiative to drive projects forward. Collaboration and Communication Skills: Excellent verbal and written communication skills, capable of collaborating effectively with cross-functional teams and documenting workflow procedures. Quality Focus: Strong attention to detail and a commitment to maintaining high-quality standards in all automation processes. Fast-Paced Environment: Enthusiasm for working in a fast-paced startup environment, where adaptability, prioritization, and a goal-oriented mind set are essential. Education: Minimum of a bachelor’s degree in biology, engineering, or a related discipline. What You Bring: Workflow Development: Collaborate with cross-functional teams to design, build, and optimize automated workflows for various stages of biotech R&D, including RNA and DNA extractions, cell culture, and NGS sample preparation. End-to-End Automation: Create end-to-end automated solutions that streamline and accelerate laboratory processes while ensuring data integrity and quality. Data Management: Implement data storage solutions to track and manage experimental data generated through automated processes. Continuous Improvement: Stay current with industry best practices and emerging automation technologies, driving ongoing improvements in workflow efficiency and reliability. Collaboration: Work closely with scientists, engineers, and researchers to understand their automation needs and provide technical support. Documentation: Maintain detailed documentation of automated workflows, troubleshooting procedures, and standard operating protocols (SOPs). Quality Assurance: Perform quality control checks on automated processes, identifying and resolving any issues promptly. Training: Provide training and guidance to team members on using automated systems effectively. ShapeTX offers a robust benefits package, including but not limited to: Medical, Dental and Vision coverage for employees and their eligible dependents. You will thrive in our fast-paced startup environment, where autonomy, initiative, and a passion for research are essential. If you are ready to contribute to groundbreaking research, possess proven experience in biotech and pharmaceutical automation, and have a vision for optimizing laboratory processes, we invite you to apply. You will join our satellite site in Boston. We are proud to offer a competitive paid parental leave benefit, an annual employee stipend for employees to use however they choose, a Flex Paid Time Off program (allowing flexible PTO for vacation, sick leave, and other purposes) and Company paid Long Term Disability. not only through our science, but also through our commitment to foster an inclusive environment that supports diverse perspectives and experiences. Additional compensation may include annual target bonus and/or sign-on bonus, equity grant and relocation bonus.We aspire to Shape Life! You can find us at shapetx.com and on LinkedIn and Twitter.At ShapeTX, we are a dynamic team of professionals who are dedicated and passionate about making cures a reality. The ShapeTX platform enables pharma innovators to design treatments across a wide range of diseases, including rare genetic disorders as well as debilitating conditions, such as Alzheimer’s, Parkinson’s, and many more. The hired applicant's placement within the range is based on qualifications and professional experience. In this role, you will be responsible for designing and building end-to-end automated workflows and collaborating closely with cell and molecular biologists to optimize processes.
Research Associate II
Company: Belharra Therapeutics
Location: San Diego, CA
Posted Sep 19, 2023
Individual pay within that range can vary for several reasons including skills/capabilities, experience, and available budget.Belharra is committed to being an Equal Opportunity Employer and our policy is to provide equal employment opportunities to all applicants and employees without regard to race, color, creed, religion, sex, sexual orientation, gender identity, marital status, citizenship status, age, national origin, ancestry, disability, veteran status, or any other legally protected status and to affirmatively seek to advance the principles of equal employment opportunity.Privacy Act Notice and Policy Statement Belharra is a highly engaged and collaborative environment, and we are seeking likeminded colleagues. WHAT YOU’LL BE RESPONSIBLE FORCollaborate with the proteomics team to implement our high throughput chemoproteomic platform. This platform is based in live cells and combines a library of chemical probes with quantitative mass spectrometry.Enable automated systems for preparing proteomics samples, including chemical probe enrichments, activity-based proteomics, MS-based quantities strategies (TMT, SILAC, DIA).Prioritize tasks to support multiple and parallel projects.Manage tissue culture demands (including multiple cancer cell lines and primary cell models).Basic understanding of mass spectrometry-based software (Proteome Discover, Skyline).WHAT YOU’LL BRING TO THE TEAMBachelor’s degree with 2-6 years of experience or master’s degree with 0-3 years of experience in fields like chemical biology, biochemistry, or cell biology (industry experience is a plus).Hands-on experience with molecular biology techniques (SDS-PAGE, western blotting), cell culture, and proteomic sample preparation.Familiarity with high-throughput or automated assays.Basic knowledge of characterizing small-molecule and protein identification.Understanding of proteomics sample processingFamiliarity with small-molecule pharmacology, chemical biology, and basic chemical principles is advantageous.Strong troubleshooting and problem-solving abilities.Attention to detail and good documentation practices.Excellent oral and written communication skills.Proficient in Microsoft Office applications.Ability to work both independently and as part of a team in a fast-paced learning environment.A strong team player that enjoys drug discovery and making a meaningful impact to drive projects forward.Physical DemandsLifting of 20-30 pounds of equipment.WHAT YOU’LL GET AS PART OF OUR TEAMA collaborative and positive culture Limitless growth and learning opportunitiesCommitment to talent and leadership developmentAll Belharrans gain access to the SkillCycle platform and receive the opportunity to work 1:1 with a coach to support their growth and developmentA chance to make a lasting impact on drug discovery and human healthCompetitive compensation and company ownershipExcellent Medical, Dental and Vision coverage from a broad choice of providers and plans 100% of premium coverage for employees; up to 95% of premium coverage for eligible dependents401(k) program with a company sponsored contribution“Take what you need” vacation and sick time off policy10 annual paid company holidays, plus the last week of DecemberA new office and lab space in San Diego with flexibility and autonomy to do your work how and where you needPay Scale Range (CA)$76,000—$93,000 USDAt Belharra Therapeutics, Inc. pay ranges are subject to change and are assigned to a job based on its level within the company. Our aim is to deliver transformative, first-in-class medicines for patients suffering from the most serious diseases. WHAT WE ARE LOOKING FORBelharra is seeking a motivated Research Associate II to join our Proteomic team and develop and support a robust chemoproteomic platform. In this role, you’ll collaborate with chemists and biologists to create and use chemical tools to enable drug discovery. The successful candidate will have a background with high-throughput proteomic sample preparation and expertise in mass spectrometry. This role will contribute to the growth of Belharra’s research portfolio by screening our chemical probe library to identify and characterize interactions with proteins of interest in a variety of cell-based assays. Through the application of our proprietary chemoproteomics platform merged with innovative biology and medicinal chemistry, we are modulating protein function in previously unidentified ways to push the limits of drug discovery. WHO WE AREBelharra Therapeutics is an early-stage small molecule discovery company founded by pioneers in the field of chemical biology.
Senior Analyst, QC Microbiology (Contract)
Company: Allogene Therapeutics
Location: East Bay
Posted Sep 18, 2023
Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. Maintains working relationships with peers, department management, and other departments (e.g, QA, Facility & Engineering, and Manufacturing). Contributes toward the development, revision, application, maintenance, validation and review of methods SOPs. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law.As an equal opportunity employer, Allogene is committed to a diverse workforce. degree in a scientific discipline or equivalent experienceExperience in a cGMP compliant environment or equivalent combination of education and experienceDemonstrated knowledge in “core” microbiological laboratory techniques including aseptic techniques, EM sampling and testing, LAL, Sterility, Bioburden, Growth Promotion, TOC, etc.Previous working experience in aseptic techniques and EM/Microbiological methods is required Experience in maintenance of GMP laboratory, laboratory equipment, and the status of pipettes and supplies. Able to perform QC laboratory maintenance related duties as assigned Experience supporting Invalid, OOE, and OOS investigations and CAPA initiationExperience authoring SOPs , EM trend reports, and validation protocolsExperience with LIMS (e.g.,MODA) and Sterility test isolators is plusAble to follow instructions and SOPs precisely and able to keep accurate and contemporaneous documentationAble to learn new skills rapidly and achieve proficiency. Position Requirements & Experience:A minimum B.S. Responsibilities include, but are not limited to:Performs EM /Micro QC sampling and testing to support the release of utilities, facility and productSupport special studies such as microbiological method suitability testingSupport implementation of EM IT System (MODA) and LIMSMaintains compliance status of laboratories by monitoring equipment, instruments, EM plates, reagents and ensuring adherence to GMP requirementsMaintains availability of laboratory supplies EM plates, media, reagents by monitoring inventories closely.Manages EM and Utility sampling and testing schedule and chain of custody of samplesPerforms all activities in accordance with cGMP requirements and reports discrepancies. Initiates and completes laboratory discrepancy events within expected timelines.Documents testing activities and results, ensuring completeness and accuracy per cGMP.Demonstrates hands-on knowledge of operation, maintenance and troubleshooting of instruments as well as GMP requirements pertinent to quality control labs. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients.
(Senior) Platform Science Manager
Company: Click Therapeutics
Location: Boston, MA
Posted Sep 17, 2023
This position is based out of Click's headquarters located in Tribeca, NYC, or one of our industrious office in either Boston, MA, Miami, FL or Berlin, Germany. Click Therapeutics will conduct interviews face-to-face over Zoom. 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 U.S. and, if so, whether that authorization permits them to work in the job they seek. 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. The final base salary will be dependent upon skills, experience and location. If you have any questions regarding the validity of a recruitment inquiry or an interview, please contact the Click's recruitment team at [email protected] to confirm before proceeding. This role will be a part of the larger Medical Office at Click comprising platform science, clinical development and operations, medical affairs, and clinical strategy and innovations. In addition to the base salary, Click Therapeutics offers an annual performance-based cash bonus and a generous equity package.BenefitsThe role includes great benefits and is an excellent wealth-building opportunity at a fast-growing pre-IPO company in a nascent and extremely exciting space.Competitive Salary with Annual Review | Cash Bonus | Stock Options | 5% 401(k) matching | Medical | Dental | Vision | Life Insurance | Voluntary Benefits | Unlimited PTO | Uber One | Nectar Rewards | One Medical | Fertility Support | Fitness Reimbursement | Bike Membership | Professional Development Stipend | Lunch Stipends | Parent Benefits | Industrious Workspaces | Commuter Subsidies | Flexible Work Arrangement | Choice of Mac or Windows | Sponsored Company Events | Office Snacks and Beverages | Much More...Equal Employment OpportunityClick 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. Responsibilities Manage clinical scientists responsible for digital therapeutic development Defining Click's clinical AI/ML research strategy advancing personalized, proprietary, targeted, evidence-based, prescription digital therapeutics Cross-functional collaboration with Click's medical, product, tech, and data teams Ensure integration of clinical AI/ML research into the larger Click data platform Manage development of digital biomarkers and closed-loop therapy to support Click's growing portfolio Build and manage the Clinical AI/ML Research team Stay on top of the AI/ML state-of-the-art and help identify new opportunities Qualifications A PhD degree in neuroscience, computer science, biomedical or control engineering, clinical science, or related field Experience designing and conducting clinical and real-world evidence trials At least 3+ years of post-degree experience (industry preferred) conducting clinical AI/ML research At least 3 years experience with direct management of research teams or interfacing with cross-functional stakeholders Experience with data collection, data mining and/or data assimilation and biomarker development Experience with the AWS ML stack Hands on experience with data science and ML/AI methods A creative and interdisciplinary approach to R&D Excellent interpersonal and communication skills Preferred Qualification Clinical experience with indications in our pipeline Prior experience with digital therapeutics Proficiency and fluency in programming (e.g., Python) and data manipulation (e.g., SQL, Pandas, Snowflake) Proficiency with physiological, actigraphy, or mobile sensor signal processing Experience working within a regulated company and understanding of privacy and security regulations (e.g., GDPR, HIPAA), and their implications for modern ML systems Compensation:The base salary range for this position is between: $100,000 - $150,000.
Scientist/Scientist II, Research Technologies
Company: Shape Therapeutics
Location: Boston, MA
Posted Sep 16, 2023
Employees are eligible to enroll in our Company’s voluntary 401k plan, voluntary Life/AD&D and Voluntary FSA’s.The salary range for the Scientist role is $96,000-$144,000. Meet some of the team members here.What You’ll Do: Assay Optimization: Work collaboratively with our Automation Engineer to optimize cell and molecular biology assays for automation, ensuring accuracy and reliability. Workflow Integration: Collaborate closely with the Automation Engineer to integrate optimized assays into automated workflows, streamlining laboratory processes.Data Analysis: Analyze and interpret data generated from automated experiments, identifying areas for improvement and refinement, and make data-driven decisions.Problem Solving: the ability to quickly diagnose problems, identify solutions, and maintain a can-do attitude.Documentation: Maintain comprehensive documentation of assay protocols, automation processes, and troubleshooting procedures.Collaborative Research: Collaborate with cross-functional teams of scientists to contribute to cutting-edge research projects.Continuous Improvement: Stay updated on the latest advancements in cell and molecular biology and automation technologies, recommending and implementing improvements to assays and processes.Quality Assurance: Implement quality control measures to ensure the accuracy and reliability of automated assays. What You Bring: Cell and Molecular Biology Expertise: A strong background in cell and molecular biology, with hands-on experience in assay development, cell culture, molecular techniques, and NGS. Automation: Experience and familiarity with automation systems and the ability to collaborate effectively with an Automation Engineer to integrate assays into automated workflows. Collaboration: Proven ability to work collaboratively in cross-functional teams, particularly with Automation Engineers, to optimize and automate laboratory processes.Detail-Oriented: Meticulous attention to detail and a commitment to producing high-quality, reproducible results.Analytical Skills: Proficiency in data analysis and interpretation, with the ability to troubleshoot and refine assays for improved performance.Problem-Solving: Strong problem-solving skills and the ability to adapt assays to meet specific research needs.Communication Skills: Excellent communication skills, both written and verbal, to document experimental procedures and collaborate effectively with team members.Innovation: A passion for innovation and a desire to push the boundaries of scientific research through automation.Education & Experience: A PhD in Biology or a related discipline. We are proud to offer a competitive paid parental leave benefit, an annual employee stipend for employees to use however they choose, a Flex Paid Time Off program (allowing flexible PTO for vacation, sick leave, and other purposes) and Company paid Long Term Disability. Thriving in a fast-paced startup environment, characterized by autonomy, initiative, and a shared passion for research, along with excellent communication and collaboration is essential to excel in this role. Non-PhD candidates with 5-10+ years of at-the-bench experience and demonstrated success within the biotech industry will be considered. ShapeTX offers a robust benefits package, including but not limited to: Medical, Dental and Vision coverage for employees and their eligible dependents. not only through our science, but also through our commitment to foster an inclusive environment that supports diverse perspectives and experiences. Additional compensation may include annual target bonus and/or sign-on bonus, equity grant and relocation bonus.We aspire to Shape Life! Additionally, maintaining a can-do attitude even in the face of technical challenges will be a valuable asset to our team's success. You will join our satellite site in Boston. The hired applicant's placement within the range is based on qualifications and professional experience. You can find us at shapetx.com and on LinkedIn and Twitter.At ShapeTX, we are a dynamic team of professionals who are dedicated and passionate about making cures a reality.
Director of Payer Marketing
Company: CymaBay Therapeutics
Location: North Jersey
Posted Sep 16, 2023
The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. CymaBay is a multi-state employer, and this salary range may not reflect positions that work outside of the Bay Area or in other states. The role will work closely with the national account team and with trade and specialty distribution to ensure optimal access and availability of seladelpar for patients with liver disease.This is a hybrid role - our work from home days are Monday and Friday and our in-office days are Tuesday, Wednesday and Thursday.Role and ResponsibilitiesDevelop and lead the execution of the payer marketing strategy, the distribution network design strategy, and tactical plans associated with both to successfully launch seladelpar in the US.Partner with commercial operations to deliver market insights through primary and secondary research that inform market access workstreams including access, distribution, pricing, contracting and forecast assumptions.Provides strategic direction and customer perspective on development of internal/external/coverage/reimbursement strategies, education, tools and support.In collaboration with the national account team and medical affairs, determine the value platform and appropriate commercial tactical plan for payers including branded and above brand messages.In collaboration with the trade and specialty distribution and patient support services, determine the network design strategy and appropriate tactical plan and materials that will ensure the optimal patient experience.Set direction for communication strategies to keep internal management team regularly informed about coding/coverage/reimbursement issues affecting the company and its customers.Partner with brand marketing to ensure alignment of commercialization strategy, launch campaign and tactical plans that deliver rapid, broad, and profitable access.Select and manage payer consulting and advertising partners and other vendors as needed.Build and optimally manage market access promotion budget to balance goals of optimizing return on investment and driving launch performance.Core Competencies10+ or more years’ experience in pharmaceutical or a combination of experience in related areas such as healthcare sales, market access, provider marketing, patient access or reimbursement.Strong knowledge of the pharmaceutical marketplace and deep understanding of the pharmaceutical industry and broader trends in healthcare landscapeCreative and experienced at developing and executing payer strategies.Working knowledge of current US payer landscape and government dynamics, including commercial and Medicare Part D plans.Demonstrated strong communication and collaboration skills with an ability to navigate a matrix environment with different cultures and disciplines.Results-driven and takes initiative and ownership to accomplish work independently.Ability to demonstrate flexibility and embrace change in a dynamic, rapidly growing environment shifting from clinical development to commercial deployment.Strive for continuous improvement and embrace innovative ideas into daily work.High analytical capability with history leveraging market research and recommending appropriate KPIs.Strong financial background in building forecasts and responsibly managing marketing budgets.Demonstrated partnership with medical, legal and regulatory functions to develop compliant tactics aligned with pharmaceutical regulatory requirements.QualificationsBS or BA in a relevant scientific discipline, MBA preferred.Liver disease or specialty disease area experience preferred.Launch and start-up experience preferred.Ability to travel domestically depending on business needs.The anticipated salary range in Newark, California is $235,000 - $260,000. The Director of Payer Marketing reports to the Vice President of Market Access and will be responsible for the commercialization strategies for market access.
Senior Counsel
Company: Spark Therapeutics, Inc.
Location: Philadelphia, PA
Posted Sep 18, 2023
Provide transactional support for manufacturing, supply, logistics, real estate, facilities and other related agreements. will also be considered. Experience prior to receiving a J.D. Key Skills, Abilities, and Competencies Excellent analytical, problem-solving, and communication skills Strong collaboration, critical thinking, and negotiation skills to influence cross-functional teams Proven experience building and cultivating relationships with key partners and stakeholders across all organizational levels Able to thrive in a fast-paced environment and successfully manage multiple deadlines Abiding interest in and knowledge of the burgeoning gene therapy industry Spark Therapeutics does not accept unsolicited resumes/candidate profiles from any source other than directly from candidates. Responsible for providing practical and timely legal guidance on issues related to manufacturing & supply, quality assurance and validation, process engineering, EHS, corporate security, and corporate real estate and facilities. JD or equivalent from an accredited law school. Undergraduate degree from an accredited college or university. Education and Experience Requirements Minimum of 7 years of experience at a law firm or relevant in-house experience with a pharmaceutical, biotechnology, or contract development and manufacturing organization. Significant transactional experience, including drafting and negotiating a wide variety of agreements and the ability to influence and work collaboratively in a cross-functional setting with innovative technologies. Support legal department initiatives and projects in furtherance of the growth, innovation and culture of the department and organization.