- Integrated Resources Inc. (Foster City, CA)
- …Rehabilitation Therapy and Nursing. Job Description Job Title: Clinical Trials Management Associate Duration: 06 Months Location: Foster city, CA CTMA -Late Phase ... successful implementation and support of important Collaborative (CO) and Investigator -Sponsored Research (ISR) projects. Responsibilities: Non-Client sponsored studies: Serves… more
- Arcus Biosciences, Inc. (Hayward, CA)
- Summary The Associate Director, Clinical Quality Assurance is responsible for working with study management teams to facilitate internal and external adherence to ... and oversight of consultant auditors. This role will lead audits of investigator sites, internal functional/process audits, and audits of clinical vendors (GCP,… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- Sr. CTM Associate - Oncology, Hematology or Cell Therapy Location: United States - California - Santa Monica Job Description We're here for one reason and one reason ... Join Kite and help create more tomorrows. The Senior Clinical Trials Management Associate is a primarily an in‑house sponsor position (though some travel is… more
- Crinetics Pharmaceuticals, Inc. (San Diego, CA)
- Associate Director, Clinical Monitoring page is loaded## Associate Director, Clinical Monitoringremote type: Remotelocations: Remotetime type: Full timeposted ... our team as we transform the lives of others.**Position Summary:**The Associate Director, Clinical Monitoring, is responsible for monitoring execution and quality… more
- NCIRE - The Veterans Health Research Institute (San Francisco, CA)
- Staff Research Associate III, Supervisor Job Category: Staff Research Assoc Requisition Number: STAFF001553 Apply now Posted : December 19, 2025 Full-Time Hybrid ... Francisco, CA 94121, USA This position supports a collaborative, Multiple Principal Investigator (MPI) lab dedicated to improving women's health and sleep throughout… more
- NWRPros (Palo Alto, CA)
- …cancers. Our Client is seeking a dynamic and experienced Sr Manager / Associate Director of Regulatory Affairs. The role is responsible for ensuring the execution ... CMC documentation (eg nonclinical study reports, clinical protocols/study reports, Investigator Brochures, CMC information/data) and contribute to content as needed.… more
- Revolution Medicines (Redwood City, CA)
- …in the RAS signaling pathway. The Opportunity Revolution Medicines is seeking an Associate Director, Clinical Quality Assurance, who will play a key role within ... Support GCP audits and inspections of RevMed, Vendors, and clinical investigator sites by regulatory authorities or business partners. Build positive professional… more
- Gilead Sciences, Inc. (Foster City, CA)
- Associate Director, Regulatory Affairs - Virology At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as ... their aspirations. Join Gilead and help create possible, together. As an Associate Director, Global Regulatory Affairs, you will act as the Regional Regulatory… more
- Gilead Sciences, Inc. (Foster City, CA)
- …amendment, and routine submissions (eg, Development Safety Update Reports / DSURs, Investigator Brochure/ IB updates, etc.). Oversees and approves the authoring of ... conflict resolution skills. When needed, ability to travel. Job Requisition ID R0046196 Full Time/Part Time Full-Time Job Level Associate Director #J-18808-Ljbffr more
- IQVIA LLC (Carlsbad, CA)
- …requisition id: R1482206Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial ... all site documents are filed in the Trial Master File (TMF) and Investigator 's Site File (ISF) per GCP/ICH and local regulations. Reporting: Generate visit reports,… more
