We're looking for a Regulatory Affairs Specialist III, working in the Pharmaceuticals & Medical Products industry in Bridgewater, New Jersey, United States.
Contributes to the development and oversees the successful implementation of regulatory strategies for assigned products, including submission and maintenance activities related to BLA applications.
Leads and/or participates on multi-disciplinary matrixed project teams that work to project deadlines while adhering to regulatory requirements for products and/or projects.
The pay range we are offering is 35 to 40 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
Bachelor's degree from an accredited four-year college or university (Area of specialization in Life Sciences)
Knowledge and understanding of complex medical and scientific subject matter
Ability to work well within cross-functional teams
Solid oral communication and writing skills
Understanding of the US pharmaceutical market place, and familiarity with medical terminology
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.