What are the responsibilities and job description for the Senior Director, Regulatory Affairs position at Proclinical Staffing?
Senior Director, Regulatory Affairs - Perm - Boston, MA
Proclinical is seeking a dynamic and strategic leader for the role of Senior Director of Regulatory Affairs. This role is pivotal in driving regulatory efforts for vaccine development programs.
Primary Responsibilities:
The successful candidate will manage the full lifecycle of global regulatory submissions and approvals, ensuring compliance across major markets.
Skills & Requirements:
- Strong background in regulatory strategy, particularly in the field of infectious diseases and vaccines.
- Proven experience in leading regulatory meetings and securing approvals.
- Ability to manage complex regulatory portfolios.
- Strong leadership skills and strategic thinking.
The Senior Director, Regulatory Affairs' responsibilities will be:
- Develop and execute regulatory strategies for vaccine development programs.
- Manage relationships with global health authorities.
- Ensure product compliance across major markets.
- Guide regulatory teams and manage submissions.
- Mitigate risks while ensuring alignment with organizational priorities.
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.
