Safety and Pharmacovigilance Specialist - Bethesda, MD | Biospace
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Safety and Pharmacovigilance Specialist

Technical Resources International Inc.

Bethesda, MD
Posted Date:
Position Type:
Full time
Job Code:
Required Education:
Medical Doctor
Areas of Expertise Desired:
MD, Pharmacovigilance,

Job Description

Founded in 1979, Technical Resources International, Inc. (TRI) provides a unique range of support services in the areas of Communications, Health and Information Technology to both private industry and government agency clients.  TRI is currently seeking a Safety and Pharmacovigilance Specialist to join our Bethesda, MD team.

The Safety and Pharmacovigilance Specialist will perform various tasks in support of clinical research including adverse event analysis and processing, serious adverse event reconciliation, preparation of IND safety reports for submission to the FDA, safety document or data analysis, and clinical trial site support.  



•   M.D. from a U.S. accredited institution with active U.S. medical license required
•   Infectious disease and/or oncology subspecialty highly preferred
•   Knowledge of GCP and ICH guidelines preferred
•   Drug development/clinical trial experience essential
•   Knowledge of CTC and/or MedDRA coding preferred
•   Experience leading clinical and cross functional teams is a plus
•   Must have excellent oral, written, presentation and computer skills
•   2+ years of pharmaceutical or biotech industry or academic experience

Submit resume and salary requirements to:  Attn: AE, TRI, 6500 Rock Spring Dr, Suite 650, Bethesda, MD 20817, or fax to (301) 897-1702, or click Apply Now to submit.

Technical Resources International is fully committed to Equal Employment Opportunity and to attracting, retaining, developing and promoting the most qualified employees without regard to their race, gender, color, religion, national origin, age, physical or mental disability, veteran status, or any other characteristic prohibited by state or local law.