- Catalent Pharma Solutions (San Diego, CA)
- …pre-production teams in the management and successful delivery of assigned Projects for our Clinical Supply site . The Associate Project Lead serves as a liaison ... **Associate Project Lead, Pre-production** **( Clinical Supply)** **Position Summary:** + **Work Schedule:** Monday-Friday,...+ **Work Schedule:** Monday-Friday, core hours 8am-4:30pm + 100% on- site (San Diego) Catalent, Inc. is a leading global… more
- IQVIA (Los Angeles, CA)
- …pipeline to investigators in company-sponsored interventional research. + Engage with clinical trial site investigators and staff to understand ... to support clinical trial enrollment. + Provide support to company clinical development and operations teams through site recommendations, initiation visits,… more
- BeOne Medicines (Emeryville, CA)
- …contractual guidelines * Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review ... within scope of role to provide best practice and/or support to junior clinical staff. **Supervisory Responsibilities:** * Provides site level management for… more
- Oracle (Sacramento, CA)
- …and system performance Healthcare & Informatics Expertise * Deep understanding of clinical workflows, informatics principles, and site readiness requirements * ... **Job Description** Overview: The Site Project Manager is responsible for local ...(preferred) * 5+ years of experience in healthcare IT, clinical informatics, or EHR implementation/project management (required) * Experience… more
- Oracle (Sacramento, CA)
- …perfectly with both project objectives and specific site requirements. + ** Site Readiness Leadership** : Offer your clinical expertise and leadership to ... **Job Description** **Oracle Health Government Services** **Lead Clinical Consultant** **Location: United States** **No visa sponsorship...content, and tailoring it to meet specific project and site needs. You will be at the heart of… more
- Pfizer (South San Francisco, CA)
- …study level informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other ... responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for...requiring you to live within commuting distance and work on- site an average of 2.5 days per week. The… more
- Gilead Sciences, Inc. (Foster City, CA)
- …of clinical research experience in the biotech or pharmaceutical industry (eg, clinical development, site management, site monitoring, clinical ... **Associate Director, Risk Based Quality Management (RBQM)** **Global Development | Clinical Operations** Clinical Operations is responsible for the worldwide… more
- Norstella (Sacramento, CA)
- …+ Clinical development planning and forecasting + Protocol Design, Country, Site and Investigator Feasibility + Clinical trials operations, cost benchmarking ... trial landscape (Clin Dev/Ops, clinical development plan development, clinical trial design, feasibility and site selection, protocol design, etc)… more
- Ascendis Pharma (Palo Alto, CA)
- …program + For clinical trials: design, provide overall oversight, and support site and subject retention + Serve as a Medical Monitor for clinical ... clinical trial protocols, investigator brochures, medical monitoring plans, site training materials, clinical study reports, health authority responses,… more
- Ascendis Pharma (Palo Alto, CA)
- …consider a remote arrangement for the right candidate. Key Responsibilities + For clinical trials: design, provide oversight, and support site and subject ... retention + Ensure successful completion of documents (including clinical trial protocols, investigator brochures, monitoring plans, site training materials, … more