Part-Time VP, Regulatory Affairs — FDA Submissions

PPG US ProPharma Group, LLC; Raleigh (NC); Hybride; USD 120 000 - 180 000; Temps partiel

Résumé du poste

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.

Responsabilités

• 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.

Connaissances

Regulatory strategy

FDA interactions

Cross-functional leadership

Regulatory submissions

GxP / compliance

Formation

Master's degree in life sciences

Regulatory affairs certification

Description du poste

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.