About Culture & Careers Regulatory Strategy Director

Regulatory Strategy Director

Location: Multiple states

Type: Full Time

Minimum Experience: Experienced


Camargo Pharmaceutical Services is excited to announce that we are now seeking a Regulatory Strategy Director. The Regulatory Strategy Director will assess the scientific, medical, regulatory, and commercial viability of drug development opportunities and coordinate resources to systematically build and execute complete development plans that align with client business strategies.

Who You Are

  • You love working with people. You are collaborative, upbeat, and optimistic.
  • You strive for operational excellence and provide outstanding internal and external service.
  • You are a problem solver with a can-do, roll-up-your-sleeves spirit.
  • You are exceptionally organized, detail-oriented and self-directed.
  • You are a proactive and clear communicator.


What You’ll Do

As the Regulatory Strategy Director, you’ll set drug development or other regulatory strategies to support client goals and conduct and supervise research to test and validate the viability of strategic options. You will proactively troubleshoot problems and identify resources to resolve issues. As Director, you’ll supervise a Regulatory Science team and will be responsible for building the talent and skills needed for Camargo success, facilitate career advancement by providing and instilling a full understanding of projects and associated responsibilities, and provide effective coaching and performance feedback on both strengths and opportunities of team members.



  • Knowledge and skills at a level normally acquired through the completion of a Master’s or PhD in a scientific or life sciences field; 10+ years of regulatory strategy related experience preferred.
  • Demonstrated competencies of strategic thinking and influencing, innovation, initiative, project management, and leadership.
  • Ability to lead and work in cross-functional, matrixed teams with demonstrated experience in team leadership and motivation of staff to successfully execute regulatory strategies.
  • Ability to travel 10-15%, including inter-office travel.


This position can be based in either the Cincinnati or Durham office.

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About Camargo Pharmaceutical Services

We are a fast growing, global organization with a small company feel, comprised of high performing, multi-disciplinary, collaborative teams. We value independent thinking, learning and development (both personally and professionally), and provide the needed resources for you to reach your potential and goals. Camargo partners with companies in more than 25 countries worldwide and has led the largest percentage of 505(b)(2) submissions of any team submitting to the FDA—Camargo is the industry authority in 505(b)(2). Routinely holding three to six pre-IND meetings a month, Camargo has guided more than 200 FDA approvals and works with product developers across more than 25 countries.

Camargo Pharmaceutical Services provides comprehensive drug development solutions, specializing in customized programs including the 505(b)(2) pathway.

9825 Kenwood Road,
Suite 203
Cincinnati, OH 45242
Durham Office
2505 Meridian Parkway,
Suite 150
Durham, NC 27713
Phone 513.561.3329
Toll Free 888.451.5708
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