Associate Director/Director, Regulatory Affairs - Permanent - Florham Park - New Jersey

Proclinical 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

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.