- AbbVie (Irvine, CA)
- …development plan based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business ... research with appropriate supervision. + At least 5 years of clinical study experience in the pharmaceutical ...support a global scientific and business strategy. + Knowledge of clinical trial methodology, regulatory and compliance … more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …Qualifications** + Advanced scientific degree (ie, MD, PharmD, PhD) and 8+ years of biotech/ pharmaceutical industry experience OR + Master's Degree and 10+ years ... + Develop and maintain US governance frameworks to support compliance , quality, and risk management. + Support the Medical... of biotech/ pharmaceutical industry experience OR + Bachelor's… more
- BeOne Medicines (San Mateo, CA)
- …You will serve as the subject matter expert (SME) and strategic leader driving compliance , efficiency, and a culture of quality throughout the enterprise. This ... **General Description:** Senior Director , Business Process Owner (BPO) for GxP processes,...ICH Q10 / E6) and business objectives. **Essential Functions of the job:** + Own the Validation and Manufacturing-related… more
- AbbVie (Irvine, CA)
- …diverse groups within the organization and external partners * Knowledge of pharmaceutical development processes, including lead characterization, target ... and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across… more
- AbbVie (South San Francisco, CA)
- …Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business ... Director leads the direction, planning, execution, and interpretation of clinical trials or research activities of ...subspecialty fellowship is desirable. + At least 3 years of clinical trial experience in the pharmaceutical … more
- Bristol Myers Squibb (San Diego, CA)
- …Initiated Trial (IIT) program with functional area oversight to ensure quality of work and appropriate compliance with regulatory requirements + Conduct ... cell therapy, this is work that transforms the lives of patients, and the careers of those...to be the global leader in radiopharmaceuticals . The Director , Medical Affairs Research Operations, plays an integral role… more
- AbbVie (Irvine, CA)
- …in the pharmaceutical industry, academia, or equivalent. + Knowledge of clinical trial methodology, regulatory and compliance requirements in Aesthetic ... Responsibilities: + Based on strong medical and scientific experience, knowledge of compliance and regulatory requirements, Allergan Aesthetics customers,… more
- ThermoFisher Scientific (San Francisco, CA)
- … of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our ... full alignment with both customers and regulatory authorities to deliver flawless compliance . **Qualifications** + Blend of strategic and operational expertise… more
- BeOne Medicines (San Mateo, CA)
- …implementation and usage are fit for purpose and upholding the highest levels of data integrity and compliance . + Support the Global Quality leadership ... **General Description:** The Senior Director , Digital Quality Management Systems (QMS) Strategy and...Management Systems (QMS) Strategy and Operations, leads the digitalization of the QMS and supports QMS users. This role… more
- Allogene (South San Francisco, CA)
- …submissions, DMC charters, patient recruitment, clinical study monitoring, clinical compliance /SOPs, safety evaluations, preparation of statistical analysis ... professional pharmaceutical development Clinical Operations experience, with a minimum of 5 years leadership clinical trial management experience * Cell therapy… more