- Catalent Pharma Solutions (San Diego, CA)
- **Project Manager ** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... manufacturing and stability storage and testing as well as Clinical Supply Services. At Catalent San Diego, we recruit...Pharma in San Diego, CA is hiring a Project Manager who is responsible for activities associated with drug… more
- Abbott (Pleasanton, CA)
- …spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues ... you dream of. + Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO...scientists **The Opportunity** We are seeking a **Regulatory Affairs Manager ** to join Abbott's Heart Failure Division on-site in… more
- UCLA Health (Los Angeles, CA)
- …the Ambulatory CMO is forming its inaugural team and is seeking a Senior Project Manager to help shape its foundation. We are looking for a Senior Project Manager ... enthusiasm. As a key member of this growing team, the Senior Project Manager will lead the planning, execution, and refinement of high-impact initiatives that… more
- AbbVie (South San Francisco, CA)
- …area. This role must effectively interface with Statistics, Data Sciences, Medical Writing , Regulatory Publishing and Development Operations. Responsibilities + ... activities. Key Stakeholders * Directors of Statistics * Data Scientists * Medical Writers * Regulatory Publishers * Clinical Project Managers Additional… more
- AbbVie (South San Francisco, CA)
- … of Statistical Programming must effectively interface with Statistics, Data Sciences, Medical Writing , Regulatory Publishing and Clinical Operations. ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Manager of Statistical Programming is a strategic role which… more
- BeOne Medicines (Emeryville, CA)
- …play a critical role in safeguarding the integrity, safety, and quality of clinical research processes and data. This position requires: + Extensive knowledge and/or ... ICH GCP and applicable global & local regulations and guidance for clinical development. + Strong global mindset and knowledge about regulations (specific expertise… more
- Sumitomo Pharma (Sacramento, CA)
- …across the SMPA organization including, but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data Management and ... safety report activities including data compilation and analysis as well as writing of assigned sections (with vendor support.) + Compile agenda, data, slides,… more
- UCLA Health (Porter Ranch, CA)
- …the medical front and back office staff + Coordinating clinical services + Providing daily administrative and operational oversight + Providing physical ... social, cultural, and economic backgrounds. + Working knowledge of medical terminology. + Writing skills to prepare accurate and concise reports and memorandums… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …members of the global regulatory team (GRL, regional leads, CMC-RA, labeling, medical writing , regulatory operations, etc.) to develop global regulatory plans, ... 2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, quality assurance, etc.) in pharmaceutical or healthcare… more
- Stanford Health Care (Palo Alto, CA)
- …reviewing and analyzing information, identifying problems, recommending solutions, and writing reports. + Cultivates and provides exemplary customer service, ... development through regular performance appraisals. + Tracks the flow of medical records and patient information through the clinic. **Education Qualifications** +… more