Clinical Laboratory Scientist (Chemical Hygiene & Safety Officer) Lighthouse Lab ServicesClinical Laboratory Scientist (Chemical Hygiene & Safety Officer)Richmond, CAAs the Chemical Hygiene & Laboratory Safety Officer, you will serve as a key resource for laboratory leadership and staff, helping ensure that laboratory operations are safe, compliant, and aligned with current regulatory requirements and best practices. We are seeking an experienced Clinical Laboratory Scientist (CLS) to step into a unique laboratory safety and leadership role supporting a large public health laboratory in Richmond, California.
NewVice President, Translational Medicine & Clinical Pharmacology Rigel Pharmaceuticals, Inc.Vice President, Translational Medicine & Clinical PharmacologySouth San Francisco, CA$306,000–$365,000 / yearLead clinical pharmacology strategy and development plans for Rigel assets, including ADME, drug-drug interactions (DDIs), pharmacokinetics/pharmacodynamics (PK/PD), exposure-response, bioavailability/bioequivalence, and other studies required to characterize dose, regimen, safety, and efficacy. Advanced scientific degree (PhD, PharmD, MD, or equivalent) in pharmacology, pharmaceutical sciences, drug metabolism, toxicology, translational medicine, or a related discipline; PhD or PharmD strongly preferred for a clinical pharmacology-focused role.
Clinical project Associate Integrated Resources, IncClinical project AssociateFoster City, CaliforniaContractorDistributes updated study related documents (i.e. Investigative Brochures, package inserts) to study teams and internal departments as requested by the CTMA or CTM. Under close supervision reviews and participates in the quality assurance of data or documents including and not limited to GILDA and DataVision.
Clinical Trial Planning & Data Support LancesoftClinical Trial Planning & Data SupportFoster City, CAThe Contractor, Clinical Trial Planning & Data Support (Level C3) supports development programs by maintaining portfolio planning systems, ensuring data quality, and enabling consistent reporting across the organization. This role is aligned to Level C3 (Mid-Level Contractor / Specialist) and is expected to: Work independently within defined processes to manage planning data and system updates.
Clinical Data Associate - III* MindlanceClinical Data Associate - III*Lakeside Drive, CA$55 / hourThe Contractor, Clinical Trial Planning & Data Support (Level C3) supports development programs by maintaining portfolio planning systems, ensuring data quality, and enabling consistent reporting across the organization. This role is aligned to Level C3 (Mid-Level Contractor / Specialist) and is expected to: Work independently within defined processes to manage planning data and system updates.
Non-Clinical - Information Technology - IT Project Manager 22nd Century Technologies, Inc.Non-Clinical - Information Technology - IT Project ManagerSan Francisco, CAWorking closely with executive leadership, laboratory operations, clinical stakeholders, Health IT teams, and external vendors, the Project Manager will be responsible for governance, budget and schedule management, risk mitigation, stakeholder engagement, and transition planning to ensure a seamless relocation and successful activation of the centralized laboratory environment while supporting company's long-term strategic goals for innovation, growth, and excellence in diagnostic services. The incumbent will manage complex cross-functional efforts involving laboratory operations, equipment and automation integration, IT infrastructure, Epic Beaker and laboratory systems implementation, workflow redesign, operational readiness, regulatory compliance, and organizational change management.
Clinical Trial Planning & Data Support Net2SourceClinical Trial Planning & Data SupportFoster City, CARemote$53.96–$56.12 / hourThe Contractor, Clinical Trial Planning & Data Support (Level C3) supports development programs by maintaining portfolio planning systems, ensuring data quality, and enabling consistent reporting across the organization. Assist Program Ops Resource Manager with resource forecasting activities, including coordinating the design, development, and validation of forecasting algorithms.
Clinical Contracts Associate Integrated Resources, IncClinical Contracts AssociateFoster City, CaliforniaContractorIT Life Sciences Allied Healthcare CRO DIRECT # - (732)-844-8715 Gold Seal JCAHO Certified for Health Care Staffing "INC 5 0 0 0 's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row). Investigator Payment Generation: requires mastery of propriety clinical tracking system and ability to review and understand payment schedules and terms enter data and generate site payments on determined cycles.
Regulatory Operations Assistant Integrated Resources, IncRegulatory Operations AssistantFoster City, CaliforniaFull timeIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. Job Responsibilities and Skills: Disclosures work is performed under the close supervision of more senior staff following detailed instructions with well-defined procedures.
Clinical Project Associate II Integrated Resources, IncClinical Project Associate IIFoster City, CaliforniaContractorAssist in the maintaining clinical information and training of Clinical Operations personnel in the clinical trials database (GILDA). Assist with the planning and facilitation of investigator meeting and, when applicable, provide on location support during the meetings.
Clinical Project Assistant Thorough GroupClinical Project AssistantSan Francisco, CaliforniaThe Clinical Project Assistant will play an important role in keeping study activities organized and on track, maintaining high-quality clinical documentation, supporting the Trial Master File, coordinating study meetings and communications, and assisting with the day-to-day operational needs of the clinical program. As the organization continues to advance its clinical development activities, they are seeking an experienced and highly organized Clinical Project Assistant (CPA) to provide operational and administrative support to Clinical Operations and the broader clinical study team.
NewClinical Nursing Director - Perioperative Services Macpower Digital Assets Edge Private LimitedClinical Nursing Director - Perioperative ServicesSan Francisco, CA$199,600–$258,280 / yearEssential Responsibilities: Collaborates with CNO and other medical center management in identifying and implementing innovative models and best practices with an emphasis on quality of care, service improvements and cost reduction. Accountable for the following areas dependent upon medical center beds and services offered: Adult Services: Med Surg, Dialysis, Clinical Dietitian, Critical Care, TCU, RT, ED if applicable.
Clinical Laboratory Scientist Lighthouse Lab ServicesClinical Laboratory ScientistSan Francisco, CALighthouse Lab Services is working with a high-growth clinical genomics laboratory in San Francisco, CA who are launching a hybrid whole genome sequencing platform. Our recruiting team has over 19 years of proven success placing job seekers in positions ranging from entry-level Medical Technologists to seasoned Laboratory Directors.
Project Manager - Gen Med Novotech Health Holdings Pte LimitedProject Manager - Gen MedSouth San Francisco, CA$140,000–$170,000 / yearIn collaboration with the Novotech Clinical Operations and Regulatory Teams, ensure high quality ethics & regulatory submissions are made and approval obtained accordingly to meet study timelines for study set up. Understand the responsibilities of Novotech as a service provider in the pharmaceutical industry and ensure all communications with external parties and performance of the study team, presents a positive professional image of the company.
Project Manager -Oncology Novotech Health Holdings Pte LimitedProject Manager -OncologySouth San Francisco, CA$140,000–$170,000 / yearIn collaboration with the Novotech Clinical Operations and Regulatory Teams, ensure high quality ethics & regulatory submissions are made and approval obtained accordingly to meet study timelines for study set up. Understand the responsibilities of Novotech as a service provider in the pharmaceutical industry and ensure all communications with external parties and performance of the study team, presents a positive professional image of the company.
NewClinical Research Coordinator II - The Nallamshetty Lab PAVIRClinical Research Coordinator II - The Nallamshetty LabPalo Alto, CAFull timeDesiredDegree in related field;Experience with grants and contracts function, clinical trial and research data management;Experience coordinating clinical research studies, recruiting research participants, collecting research data, and working with regulatory requirements;Knowledge of clinical research principles, Good Clinical Practice (GCP), human subjects protections, and research ethics gained through education or experience. The position works closely with the Principal Investigator, study team, sponsors, regulatory bodies, and research participants to ensure studies are conducted in accordance with study protocols, Good Clinical Practice (GCP), institutional policies, and federal regulations.
Senior Clinical Program Manager Revolution Medicines, Inc.Senior Clinical Program ManagerRedwood City, CA$164,000–$205,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Ability to analyze operational data, contribute with a mind on quality, timeliness and fiscal responsibility, make and drive decisions, multi-task, prioritize tasks, anticipate challenges, and execute on goals as a member of an interdisciplinary team.
Regulatory Operations Assistant – I Integrated Resources, IncRegulatory Operations Assistant – IFoster City, CaliforniaContractorCLINICAL TRIAL DISCLOSURE & TRANSPARENCY: The Disclosure &Transparency function resides organizationally within Medical Writing The Disclosures function is responsible for clinical trial registrations and result postings in ClinicalTrials.gov and the EU Clinical Trial Register. PROJECT INVOLVEMENT: Does not participate formally in cross functional teams, but may attend team meetings under direction of a more senior staff member.
Clinical Project Associate Integrated Resources, IncClinical Project AssociateFoster City, CaliforniaContractorAssists with the planning and facilitation of investigator meetings and, when applicable, provides onsite support during the meetings. • Assist in maintaining clinical information and training of Clinical Operations personnel in the clinical trials management system (GILDA).
NewClinical Trial Planner - Planisware Varite, IncClinical Trial Planner - PlaniswareFoster City, CARemote$50–$56.11 / hourWith 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services. The Contractor, Clinical Trial Planning & Data Support (Level C3) supports development programs by maintaining portfolio planning systems, ensuring data quality, and enabling consistent reporting across the organization.