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Reference # : 17-93596 Title : Scientist V
Location : Bridgewater, NJ
Experience Level : Start Date / End Date : 01/02/2018 / 06/30/2018  
Job Title: Scientist III
Duration: 6  Months
Location: Bridgewater, NJ
Client: A Big Pharmaceutical Company

  • The Pharmacovigilance Scientist (PVS) will serve as a core member of the safety team and is responsible for performing proactive pharmacovigilance activities on a product, or group of products in a therapeutic area or franchise, in partnership with the Global Safety Officer (GSO) to evaluate safety data and signals for both marketed products and products in clinical development.
  • This includes performing signal detection and safety management committee activities, authoring safety evaluations, contributing and reviewing of aggregate safety reports, assisting with ad hoc regulatory responses, facilitating signal management process for assigned products (i.e., signal tracking, data analysis, leading review meetings, presenting, etc.) in collaboration with the GSO and Pharmacoepidemiology.
  • Additionally, the PVS will support the GSO with other safety related activities associated with new drug applications / regulatory filings, benefit risk assessment and safety risk management and support activities related to risk minimization including dRMP/RMP and REMS.
  • The PVS will provide coordination and oversight to outsourced activities (i.e., signal detection reports, clinical overviews).
  • Good knowledge of pharmacovigilance practices
  • Good knowledge of US and EU pharmacovigilance regulatory requirements
  • Excellent written and verbal communication skills
  • Ability to present and critically discuss safety data in both internal and external discussions
  • Ability to evaluate, interpret and synthesize scientific data (analytical thinking)
  • Team player with ability to function in a cross-functional environment
  • Self–motivated, able to prioritize and plan effectively, and independently, with minimal supervision
  • Fluent in English (verbal and written)
  • Good moderator skills
  • Ability to navigate in databases and pull information correctly
  • Good organizational skills and attention to detail
  • Preferred 2 years with relevant experience (including industry experience) with a working knowledge of drug safety and risk management, and understanding of drug development, basic knowledge of regulatory guidelines and medical coding (i.e. MedDRA).
  • Basic knowledge of common data processing software (i.e., Excel, PowerPoint, Word) and database systems
  • Minimum Bachelors of Science or Health Care Professional (RN, BSN, Nurse Practitioner or Physician Assistant, RPh)
  • preferred advanced health care discipline degree (MDPharmD, PhD, Masters of Science, etc.) or equivalent qualification.
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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