We are looking for a Drug Safety Specialist III, working in the Pharmaceuticals & Medical Products industry in Bridgewater, New Jersey, United States.
Performs 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.
Performs self-initiated quality review within each distinct process step.
The pay range we are offering is 28 to 35 per hour. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
6-9 years of experience
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
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.