Regulatory Affairs Specialist III
3 days ago
Apply now and our proprietary system will quickly have you in front of a live recruiter.
The Opportunity
Description
We're looking for a Regulatory Affairs Specialist III, working in Pharmaceuticals and 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.
Our Client
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?
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