We're looking for a Product Safety Coordinator, working in the Pharmaceuticals & Medical Products industry in Woodcliff Lake, New Jersey, United States.
Organizes of adverse event reports for marketed and investigational products from all sources.
Evaluates clinical trial, spontaneous (post-marketing), and solicited reports of adverse events, including communication with partners and affiliates when necessary to verify completeness and accuracy.
Prioritizes workload to ensure Company and Regulatory Authority deadlines are met.
Distributes information to co-marketing partners.
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
Bachelors degree required, preferably in a scientific or medical discipline
Previous experience in data coding and retrieval skills using database technology
Knowledge of medical terminology
Prior work experience in Product Safety/Pharmacovigilance preferred
Precise attention to detail and ability to multi-task
Good communication skills, both written and verbal
Ability to work independently, and as part of a team
We're offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.
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.