Job Posting Title Clinical Trial Psych Rater - German Speaking IQVIA Holdings IncJob Posting Title Clinical Trial Psych Rater - German SpeakingSan Francisco, CARemoteOur team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews).
NewClinical Trial Psych Rater - Mandarin Speaking IQVIA Holdings IncClinical Trial Psych Rater - Mandarin SpeakingSan Francisco, CARemoteOur team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews).
Clinical Scientist Actalent IncClinical ScientistAlameda, CARemote$90–$95 / hourThe role requires close collaboration with cross-functional study teams to ensure high-quality, compliant, and timely delivery of study milestones, with approximately 80% of the workload dedicated to detailed data review. Develop and review various study protocols withminimal guidance including writing, reviewing, adjudication/resolution of crossfunctional comments, and ensuring a high-quality final document.
Senior Manager/Director Clinical Operations Lycia TherapeuticsSenior Manager/Director Clinical OperationsSouth San Francisco, CARemote$169,000–$198,000 / yearAbility to manage in a consensus environment through teamwork, trust and shared expectations, influencing strategic direction of complex global clinical operations issues, solicit information, listen well, persuade others, make important decisions and shape outcomes. Build, develop and train internal staff and external vendors, structure department for enhancing efficiency, and create a highly engaged work environment for attracting and retaining highly qualified clinical operations professionals.
Gm/Ceo, Clinical Trial Abundance Initiative EQL TechGm/Ceo, Clinical Trial Abundance InitiativeSan Francisco, CARemoteExperienced Leader: You have 5+ years of experience in health policy, research, or clinical operations, with a demonstrated track record in managing complex initiatives that produce meaningful outcomes. Facilitate the integration of community engagement and ecosystem building methodologies into clinical trial planning and execution, ensuring trials reflect real-world patient diversity.
Senior Manager/Director Clinical Operations Lycia Therapeutics IncSenior Manager/Director Clinical OperationsSouth San Francisco, CARemote$180,000–$198,000 / yearAbility to manage in a consensus environment through teamwork, trust and shared expectations, influencing strategic direction of complex global clinical operations issues, solicit information, listen well, persuade others, make important decisions and shape outcomes. Build, develop and train internal staff and external vendors, structure department for enhancing efficiency, and create a highly engaged work environment for attracting and retaining highly qualified clinical operations professionals.
Clinical Business Operations Lead Iovance Biotherapeutics IncClinical Business Operations LeadSan Carlos, CARemote$145,000–$155,000 / yearThe ideal candidate brings strong analytical and operational skills, with the ability to oversee high-level program metrics while remaining agile to support study-level needs, including document development and eTMF support, as resourcing requires. Mental: Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlines.
NewClinical Trial Manager - Contractor Arcus Biosciences, Inc.Clinical Trial Manager - ContractorBrisbane, CARemoteClinical Outsourcing: Independently manage outsourcing activities for Phase I to III clinical trials and Clinical Development functional area projects, including vendor capability assessments, RFP/RFI, selection, contract & budget negotiation, and other related tasks for the full contract life cycle, as follows: Negotiate vendor Master Service Agreements, commercial terms, and amendments. Responsible for management and negotiation of all global clinical development contract agreements (Work orders, change orders, confidentiality, HCP agreements, subcontractor agreements, and amendments thereto) in support of multiple functions (e.g., Clinical Operations, Regulatory, Clinical Supply, Data Management, etc.).
Director, Clinical Operations Jade BiosciencesDirector, Clinical OperationsSan Francisco, CaliforniaRemote$215,000–$240,000 / yearDirects the selection of CROs and other vendors (IxRS, Central Lab, ancillary/tech vendors), directs development of vendor Scopes of Work (SOW), scope changes, budgets, and vendor payments and partners with CROs and other vendors to deliver on study execution. The Director, Clinical Operations will oversee the strategic and operational execution of clinical trials, leading cross-functional teams and collaborating with internal stakeholders and external vendors.
Director Clinical Science Iovance Biotherapeutics IncDirector Clinical ScienceSan Carlos, CARemote$175,000–$225,000 / yearMay develop or provide input for clinical presentation slides and other materials for internal/external meetings and/or ongoing communications for review/discussion with CS Medical Directors/Clinical Science Physicians (e.g., investigator meetings, pre-study site selection visits, study coordinator or clinical research administrator training, study newsletters, communications to study sites, etc.). The Director Clinical Science has primary responsibilities for supporting Medical Directors/Clinical Science Physicians and Head of Clinical Science with clinical documentation, representing Clinical Science on various teams/sub-teams or other appropriate forums, supporting training of study site personnel.
Senior Clinical Scientist Jade BiosciencesSenior Clinical ScientistSan Francisco, CaliforniaRemote$175,000–$190,000 / yearJade’s pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an undisclosed antibody candidate, both currently in preclinical development. Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases.
Associate Director, Clinical Pharmacology and Pharmacometrics (Temporary) Vir BiotechnologyAssociate Director, Clinical Pharmacology and Pharmacometrics (Temporary)San Francisco, CARemote$95–$118 / hourIts clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN ® dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology is looking for an Associate Director, Clinical Pharmacology and Pharmacometrics (Temporary Staff) who will support the design, execution, interpretation and reporting of clinical pharmacology data across all stages of drug development.
Senior Director, Clinical Portfolio and Program Management Allogene TherapeuticsSenior Director, Clinical Portfolio and Program ManagementSouth San Francisco, CARemote$230,000–$270,000 / yearWork with the program team members to facilitate project/program execution from Pre-IND planning through BLA/MAA approvals utilizing project management tools and processes to maintain strategic direction, project schedule/timeline, communications, budget/cost and identify and mitigate risks. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of “off-the-shelf” CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients.
Director, Evidence Generation and Publications Freenome IncDirector, Evidence Generation and PublicationsCARemote$214,625–$305,550 / yearPlease note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. About this opportunity: Freenome is seeking a Director, Evidence Generation and Publications to lead integrated evidence-generation and publication strategies across the company's portfolio.
Senior Director, Real World Data RWD Freenome IncSenior Director, Real World Data RWDCARemote$236,300–$335,475 / yearAbout this opportunity: As the Senior Director of Real World Data (RWD), you will be accountable for defining, developing, and implementing our RWD strategy, platform, and data pipeline to transform diverse real-world datasets into regulatory-grade, research-ready assets that drive our clinical development, evidence generation, digital health products and product offerings. Specifically, the Senior Director will lead the RWD Informatics team in turning electronic health records (EHR), claims, imaging, and other RWD sources into research-ready datasets accessible by our biostatisticians,computational scientists and other end users while ensuring data quality, operational efficiency, and scalability.
Head of Engineering Recruiting From ScratchHead of EngineeringSan Francisco, CaliforniaRemoteTheir platform uses AI agents to automate complex site-level workflows, helping clinical research organizations accelerate trial activation, improve operational efficiency, and ultimately speed up medicine delivery. The founding team combines deep healthcare domain expertise with strong technical execution, and the company is entering a critical growth phase where operational excellence and engineering leadership are essential.
Director, Scientific Affairs Mirum Pharmaceuticals IncDirector, Scientific AffairsFoster City, CARemoteIdentifies, can gain access to, and develops professional relationships with thought leaders and other healthcare professionals, active and potential study investigators, and professional organizations within their assigned geography. Utilizes scientific resources to deliver impactful presentations to varying audiences and in a variety of different settings including (but not limited to) advisory boards and patient advocacy groups.
Staff Software Engineer, Applied AI ValenceStaff Software Engineer, Applied AISan Francisco, CaliforniaRemoteWorking at Valence means you'll work directly with Fortune 500 technology leaders, building expertise through the most complex enterprise deployments while gaining insight into diverse organizational approaches to AI transformation. Our clients represent the most diverse and sophisticated enterprise AI implementations globally, including Coca-Cola, Delta, Nestlé, General Mills, Schneider Electric, Deutsche Telekom, AstraZeneca, Prudential, CVS and Bristol Myers Squibb.
Medical Science Liaison Immunology - Admilparant (N. CA) Bristol Myers SquibbMedical Science Liaison Immunology - Admilparant (N. CA)San Francisco, CARemote$166,090–$201,262 / yearThe purpose of their interactions is to engage in meaningful scientific exchange that will ensure patients have access to BMS medicines, to ensure their safe and appropriate use through peer to peer discussions aligned with medical strategies and needs expressed by external stakeholders, and to facilitate research. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Medical Science Liaison, Cardiovascular - Milvexian (Northern CA) Bristol Myers SquibbMedical Science Liaison, Cardiovascular - Milvexian (Northern CA)San Francisco, CARemote$166,090–$201,262 / yearThe purpose of their interactions is to engage in meaningful scientific exchange that will ensure patients have access to BMS medicines, to ensure their safe and appropriate usethrough peer to peer discussions aligned with medical strategies and needs expressed by external stakeholders, and to facilitate research. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.