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Safety Associate
- Permanent
- Pharmacovigilance, Good Pharmacovigilance Practice (GVP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting for a Safety Associate with a biotechnology company located in Cambridge, MA.
Job Responsibilities:
- Triage of AESI reports
- Evaluation of the existing clinical data points and generation of relevant follow-up queries for AESI reports using clinical knowledge, pharmacovigilance experience, and communication skills within predetermined timelines
- Direct administration of queries with healthcare providers in the US
- Collaboration with affiliate/distributor/and associated external AE collection partners for follow-up queries in ex-US locations
Skills and Requirements:
- Minimum of Bachelor's level degree in nursing, pharmacy, or other health care related profession or life sciences required
- 1+ year in drug safety/Pharmacovigilance in pharmaceutical industry setting or the equivalent preferred
- Minimally, a general understanding of worldwide Post-Marketing and Clinical Trial Adverse Event Regulations including GCP, CIOMS, EMA GVP
If you are having difficulty in applying or if you have any questions, please contact Janelle Jones at 267-297-3257.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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