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Reference # : 17-93580 Title : Drug Safety Specialist III
Location : Bridgewater, NJ
Experience Level : Start Date / End Date : 01/08/2018 / 07/02/2018  
Job Title: Drug Safety Specialist III
Duration: 7 Months
Location: Bridgewater, NJ
Client : A Big Pharmaceutical Client

  • Responsible for the collection, data entry, routing, follow-up, and timely reporting/submission of safety information related to drug products from a variety of sources (clinical trial, spontaneous, literature), both U.S. and foreign, in compliance with SOPs, US regulations, and international regulations. 
  • This position is also responsible for self-initiated quality review within each distinct process step.
  • Routine safety surveillance/signal detection
  • Labelling
  • Medical literature review
  • Contribution to/Creation of regulatory responses
  • Review of outsourced reports
  • Excellent verbal and written English communication skills
  • Global pharmacovigilance experience
  • Consumer health background
  • Flexible to working with many different compounds
  • Ability to make quick assessments to meet strict deadlines
  • Medical writing/literature review experience
Health care professional, ideally physician

6 to 9 years.

 Please apply on our company website ( with reference to job ID, or share your most updated resume at

Ridhi Thapa
Pharma Recruiter
Artech Information Systems LLC
360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960
Office: 973.295.4583 | Fax: 973.998.2599
Email: | Website:
About Artech Information Systems LLC
Artech is an employer-of-choice for the last 25 years to over 7,500 consultants across the globe. We recruit top-notch talent for over 70 Fortune and Government clients coast-to-coast across the U.S., India, and China. We are #1 Largest Women-Owned IT Staffing Firm in the US and this may be your opportunity to join us! For more check:

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