No more applications are being accepted for this job
- Complete drug safety monitoring and tracking in accordance with pharmacovigilance and related standards, regulations and Standard Operating Procedures
- Review, evaluate, and verify potential adverse event information during preliminary assessment to determine required action per internal policies and perform data entry of adverse event
- Perform labeling assessment for adverse events received using clinical knowledge and conduct follow up for all reported cases
- Health Care Professional degree required with 2 plus years of experience with a biotech or pharma company
- Science or Medical writing experience required
- Ability to interact effectively in a multidisciplinary team setting
- $29.00 to $31.80/hour (Dependent on Experience)
Pharmacovigilance Clinical Associate - South San Francisco, United States - R&D Partners
Description
Our biopharmaceutical client in the San Francisco Bay Area is recruiting for a Pharmacovigilance Clinical Associate.
Overview:
Requirements:
Pay Scale:
R&D Partners is a specialist employment agency and recruitment business providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
R&D Partners is an equal opportunity employer.