- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …in therapeutic products and areas; medical coding; safety-data administration + Pharmacovigilance Specialist should possess autonomy and sense of responsibility, ... and regions. **_Job Summary:_** Provides operational support for global pharmacovigilance activities of Grifols marketed products. Ensures pharmacovigilance … more
- United Therapeutics (Annapolis, MD)
- …and compliance with respect to ISCR processing and reporting. The Lead Pharmacovigilance QC Specialist provides strategic oversight of end-to-end case safety ... biology, or BSN, and 8+ years of experience in pharmacovigilance in either case processing or quality assurance of...chemistry or biology, and 6+ years of experience in pharmacovigilance in either case processing or quality assurance of… more
- US Tech Solutions (CA)
- …* Perform **quality review** of **external providers'** reconciliation tasks for clinical and post-marketing ( **medical information, product complaints, and ... This role will be 100 % remote. Candidates must posses **3 to 5 years of experience** or application/environment specific knowledge to perform tasks where large quantities of information, data or documents need to be maintained or manipulated in a **structured… more
- University of Pennsylvania (Philadelphia, PA)
- …and much more. Posted Job Title Clinical Research Monitoring and Auditing Specialist (Abramson Cancer Center) Job Profile Title Clinical Research Quality ... Specialist C Job Description Summary The Abramson Cancer Center...Play a vital role in performing quality reviews of pharmacovigilance data that are evaluated and acted on by… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …, Regulatory and Marketing departments. The Knowledge Services Specialist 2, specifically participates in evaluating external information resources ... more than 110 countries and regions. **Overview:** The Knowledge Services Specialist provides an essential support function through specialized scientific, technical… more
- Merck (De Soto, KS)
- …for animals. **As a member of the Regulatory Affairs Biologics team, the Senior Specialist will lead to drive results for the responsibilities provided but is not ... Communications, Licensing Law, Medical Device Regulations, Pharmaceutical Regulatory Affairs, Pharmacovigilance , Process Improvements, Project Management, Public Affairs, Public Relations… more
- Merck (Lower Gwynedd, PA)
- …Management, Management Process, Mentorship, Pharmaceutical Regulatory Affairs, Pharmacovigilance , Regulatory Affairs Compliance, Regulatory Affairs Management, ... Regulatory Communications, Regulatory Compliance, Regulatory Experience, Regulatory Reporting, Regulatory Strategy Development {+ 4 more} **Preferred Skills:** **Job Posting End Date:** 06/5/2025 A job posting is effective until 11:59:59PM on the day**… more
- AbbVie (Florham Park, NJ)
- …be based on qualifications listed below. Purpose: The Senior Director provides specialist medical and scientific strategic and operational input into core medical ... GMA input into and influences the development of asset strategy. Provides specialist medical insights, and executes on data generation, communication, and expert… more
- Bristol Myers Squibb (Phoenix, AZ)
- …of gaps in FM resources; collaborates with the Field Medical Communication Specialist (FMCS), TA point, Medical Information and Medical Strategy on development of ... Adverse Events (AEs) and fully understand and comply with BMS Pharmacovigilance SOPs regarding identification and reporting timelines + Contributes to managing… more
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