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About Culture & Careers Regulatory Scientist

Regulatory Scientist

Location: Multiple states

Type: Full Time

Minimum Experience: Entry Level

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To meet accelerating growth, Camargo Pharmaceutical Services is seeking Regulatory Scientists with experience in providing high-quality scientific writing and advanced scientific research expertise for our cross-functional project teams overlaid with US, Europe and/or Asia regulatory understanding. These positions are located in either our Cincinnati, Ohio or Raleigh-Durham, North Carolina offices.

Since Camargo Pharmaceutical Services is the leading expert in drug development, you will provide expertise and customer-centric professionalism to our clients, which range from small biotech firms to large, established pharmaceutical companies.

This position is a natural fit if you possess well-developed and demonstrable writing skills, understand strategic communications, and can “simplify the complex.” Strategic/critical thinking skills, as well as initiative, are a must for this role! If you are inherently inquisitive and looking to get away from bench work to focus on strategic thinking, then Camargo is the place for you!


Qualifications

  • Ph.D. in a scientific or life sciences field with minimum 1+ year post-graduate experience.
  • 1+ years of industry-related experience. Prior internship experience preferred.
  • Demonstrated knowledge of the research process and direct research experience.
  • Demonstrated writing skills
  • Ability to work collaboratively in a team environment, including global companies and sponsors.
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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.


Contact
Headquarters
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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