Interim VP, Regulatory Affairs

PPG US ProPharma Group, LLC; Raleigh (NC); Hybrid; USD 120,000 - 180,000; Part time

Job summary

ProPharma is seeking an Interim VP, Regulatory Affairs to provide senior strategic and hands‑on support across development programs. You will help set regulatory priorities, lead preparation for FDA interactions and key submissions, and advise cross‑functional teams on regulatory decisions.

The role supports the organization through a period of limited capacity, with a 20‑hour workweek and a four‑month duration in a hybrid schedule in the United States.

Qualifications

• Provide senior strategic and hands-on regulatory support across development programs.
• Advise cross-functional teams on regulatory decisions to maintain alignment.
• Lead preparation for FDA interactions and key submissions.

Responsibilities

• Provide senior strategic and hands-on regulatory support.
• Help set regulatory priorities across development programs.
• Lead preparation for FDA interactions and key submissions.
• Advise cross-functional teams on regulatory decisions.
• Provide oversight to keep work moving during limited capacity.

Skills

Regulatory strategy

FDA interactions

Cross-functional leadership

Regulatory submissions

GxP / compliance

Education

Master's degree in life sciences

Regulatory affairs certification

Job description

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Interim VP, Regulatory Affairs

• to provide senior strategic and hands‑on support
• help set regulatory priorities across development programs
• lead preparation for FDA interactions and key submissions
• advise cross‑functional teams on regulatory decisions
• provide oversight to keep work moving during a period of limited team capacity
• 20 hours per week
• Hybrid Schedule (onsite work in Berkeley Heights, NJ)
• Minimal travel
• 4 months in duration

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.

ProPharma will never ask you for any bank account information, financial information, or another form of payment to be considered for a role. Additionally, the ProPharma talent acquisition team will only use their work email addresses ([e-mail]).