What are the responsibilities and job description for the Pharmacovigilance Specialist position at Primary Talent Partners?
Primary Talent Partners is looking to fill a 1 year contract role for a Global Pharmacovigilance Specialist for a large pharmaceutical client.
Responsibilities:
- Review and approve adverse event reports for pharmaceutical, biologicals and pesticide animal health products.
- Enter case data into validated database.
- Submit expedited cases to the appropriate Health Authority.
- Process and/or submit Aggregate reports as needed.
- Participate in literature search processes.
- Initiate and coordinate investigations into pharmacovigilance reports.
- Provide guidance to national pharmacovigilance teams regarding cases.
- Assist in processing and case administration tasks.
- Perform all duties in compliance with regulatory requirements, internal procedures and corporate policies.
Qualifications:
- Education minimum requirement-DVM/VMD or equivalent Required Experience and Skills-Clinical veterinary medical experience.
- Excellent interpersonal, communication and negotiating skills.
- Must be able to work effectively as a team member in a highly interactive and collaborative environment.
- Preferred Experience and Skills-Knowledge of animal health regulations of major regulatory agencies (FDA, EPA, USDA, and/or EMA).
- Experience with Microsoft Office. Strong organizational, written and oral skills.
- At least 2 years of experience in Pharmacovigilance or Regulatory Affairs in an industrial setting is an advantage.
- Hybrid role
Job Types: Full-time, Contract
Pay: $48.00 - $51.00 per hour
Schedule:
- 8 hour shift
- Monday to Friday
Education:
- Bachelor's (Preferred)
Experience:
- Pharmacovigilance: 2 years (Preferred)
- Regulatory: 2 years (Preferred)
Work Location: One location
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