- 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 ... + Knowledge of ICH, US & EU regulations, and requirements for Pharmacovigilance . + Excellent interpersonal skills, with demonstrated ability to work in a… more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …and regions. **_Job Summary:_** Provides operational support for global pharmacovigilance activities of Grifols marketed products. Ensures pharmacovigilance ... Grifols pharmaceutical products. + Contributes to ensure compliance of pharmacovigilance activities including activities such as conduct case reconciliation with… more
- Sumitomo Pharma (Sacramento, CA)
- …a dynamic, highly motivated, and experienced individual for the position of ** Associate Manager, Compliance, Training & Strategic Alliance (CTSA), PVRM** . The ... Associate Manager, Compliance, Training & Strategic Alliance (CTSA), PVRM...(CTSA), PVRM is responsible for the management of the Pharmacovigilance (PVRM) and non-PVRM vendor(s) (eg Commercial) and will… more
- United Therapeutics (Sacramento, CA)
- …are passionate about PV and enjoy being part of a collaborative team. The Associate Global PV Case Management Director plays a key role in management and oversight ... role is critical in ensuring that commercial operational aspects of pharmacovigilance activities are managed with rigorous global standards in proper documentation,… more
- Bristol Myers Squibb (Los Angeles, CA)
- …data generation, insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on managing a team ... Adverse Events (AEs) and fully understand and comply with BMS Pharmacovigilance SOPs regarding identification and reporting timelines + Contributes to managing… more
- Gilead Sciences, Inc. (Foster City, CA)
- …research through post-marketing + Strong experience in Good Clinical and Good Pharmacovigilance Practices and knowledge of evolving regulations, such as ICH E6 R3 ... + Proven experience advising business functions in the biopharma industry on quality and compliance requirements and continuous improvement + Experience working across a broad spectrum of quality and/or compliance activities, including authoring SOPs, leading… more
- Amgen (Los Angeles, CA)
- …required to gain access to therapy + Partner with Safety and Pharmacovigilance (PV). Report Adverse Event (AE)'s and product complaints through medical information ... degree OR Bachelor's degree and 2 years of Case Management experience Or related Associate 's degree and 6 years of Case Management experience Or related High school… more
- AbbVie (South San Francisco, CA)
- …and responses, and other program documents. + May oversee the work of Associate Medical and/or Scientific Directors, and of Clinical Scientists working on the same ... key regulatory discussions. + Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality… more
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