- AbbVie (South San Francisco, CA)
- …applicable regulatory requirements for work processes are met. Critically review regulatory submission documents. Participate in discussions with ... LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director, Statistics - Oncology provides statistical leadership for clinical… more
- Sumitomo Pharma (Sacramento, CA)
- …a dynamic, highly motivated, and experienced individual for the position of ** Associate Medical Director.** The Associate Medical Director will provide hands-on ... and Canadian Product Monograph (PM) + Ensures timely and quality review and assessment of ICSRs, including seriousness, expectedness, safety narratives, adverse… more
- Takeda Pharmaceuticals (Thousand Oaks, CA)
- …you will lead quality oversight to ensure that all products meet applicable regulatory and Takeda quality standards across global markets. You will oversee critical ... quality systems including batch record review , product release, change control, deviation management, and annual...annual product reviews, while driving compliance with cGMP and regulatory requirements. You will contribute in global and site-level… more
- BeOne Medicines (San Mateo, CA)
- **General Description:** + This position supports Regulatory Affairs personnel in the coordination, preparation, and submission of all INDs/NDAs/MAAs and life cycle ... ensure submission compliance for Health Authority (HA) acceptance. + Support Regulatory Affairs to deliver high quality and consistent maintenance health authority… more
- Stanford University (Stanford, CA)
- …case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board renewals are ... Clinical Research Coordinator Associate (1 Year Fixed-Term) **School of Medicine, Redwood...Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. +… more
- Stanford University (Stanford, CA)
- …case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board renewals are ... Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States**...Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. +… more
- Stanford University (Stanford, CA)
- Industrial Contract Associate **Dean of Research, Redwood City, California, United States** **New** Compliance Legal Post Date 3 days ago Requisition # 107067 ... of education, research, and operation. **POSITION SUMMARY:** **The Industrial Contracts Associate will provide essential support to Stanford faculty by drafting and… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- **Job Summary** **** The Associate Director, MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing processes ... aspects of downstream process technology transfers to CDMOs, including documentation review , gap analysis, and risk assessment. + Provide expert technical oversight… more
- AbbVie (South San Francisco, CA)
- …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director, Statistical Programming leads the whole stat programming team ... and analysis oversight for OED all clinical projects conducted by CROs. The associate Director leads the recruitment and training of new staff onboarding activities,… more
- Wells Fargo (Westlake Village, CA)
- **About this role:** Wells Fargo is seeking a Registered Client Associate in Wealth and Investment Management as part of Wells Fargo Advisors. Learn more about the ... marketing campaigns, establishing and maintaining files to meet the firm's regulatory requirements, and establishing and maintaining filing and record keeping… more