Interim Regulatory Affairs Leader (20h/Week, Hybrid)

propharmagroup; United States; Hybrid; USD 100,000 - 150,000; Part time

Job summary

ProPharma Group is seeking an Interim VP, Regulatory Affairs in Berkeley Heights, NJ. This part‑time consultant will set regulatory priorities across development programs, guide FDA interactions, and oversee cross‑functional regulatory decisions during a period of limited capacity.

The role emphasizes strategic guidance, hands‑on support, and collaboration with teams to ensure timely regulatory milestones over a 4‑month engagement, with hybrid onsite work and limited travel.

Qualifications

• Senior regulatory leadership experience preferred.
• Expertise in FDA interactions and submissions.
• Ability to advise cross‑functional teams on regulatory decisions.

Responsibilities

• Set regulatory priorities across development programs.
• Lead preparation for FDA interactions and key submissions.
• Provide oversight to keep work moving during limited team capacity.
• Advise on regulatory decisions across programs.

Skills

Regulatory strategy

FDA submissions

Cross-functional leadership

Regulatory affairs

Job description

ProPharma Group is seeking an Interim VP, Regulatory Affairs in Berkeley Heights, NJ. This part‑time consultant will set regulatory priorities across development programs, guide FDA interactions, and oversee cross‑functional regulatory decisions during a period of limited capacity.

The role emphasizes strategic guidance, hands‑on support, and collaboration with teams to ensure timely regulatory milestones over a 4‑month engagement, with hybrid onsite work and limited travel.