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ProPharma Group

Regulatory sciences consultant for life sciences

Interim Vice President Regulatory Affairs

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Part-timeNo salary listed

About the Job

Responsibilities

  • 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.

About the Company

ProPharma Group

Regulatory sciences consultant for life sciences

ProPharma Group provides regulatory sciences consulting and related services for drugs, biologics, medical devices, and diagnostics on a global scale. Its offerings cover the full lifecycle, from early development and clinical trials to regulatory approval and post-market activities. The company’s services include regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology, delivered by a team of over 2,500 professionals with more than 20 years of operation. ProPharma Group differentiates itself by providing expert, end-to-end regulatory and life sciences solutions across multiple product types and stages, helping pharmaceutical, biotechnology, and medical device companies navigate complex regulatory and compliance challenges. The goal is to help clients bring safe and compliant products to market efficiently while maintaining ongoing lifecycle support.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Raleigh, NC
Founded
2001

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