Associate Director/Director, Regulatory Affairs - Permanent - Florham Park - New Jersey
À±½·ÊÓƵ is seeking a strategic leader to drive regulatory initiatives for innovative antiviral treatments.
Primary Responsibilities:
The successful candidate will collaborate with cross-functional teams and regulatory authorities to develop and implement regulatory strategies that support global development goals. You will also manage submissions, compliance, and post-marketing activities, ensuring successful transitions from early development to commercialization.
Skills & Requirements:
- Bachelor's degree in life sciences or related field (advanced degree preferred).
- 7+ years (Associate Director) / 10+ years (Director) of regulatory experience, preferably in antiviral products.
- Strong knowledge of FDA and ICH guidelines.
The Associate Director/Director, Regulatory Affairs' responsibilities will be:
- Develop and execute regional regulatory strategies.
- Collaborate with cross-functional teams and regulatory authorities.
- Lead regulatory submissions, updates, and ensure compliance with guidelines.
If you are having difficulty in applying or if you have any questions, please contact Nicholas Walker at n.walker@proclinical.com
À±½·ÊÓƵ is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
À±½·ÊÓƵ Staffing is an equal opportunity employer.
.png)
