Regulatory Manager

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Regulatory Submissions Manager

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Are you an experienced CRA/ Site Manager/ IRB Associate looking for new opportunities in clincal research?

We are currently seeking key managers to join our Regulatory Submissions team in Clinical Operations.    

The position is an office-based position in Cincinnati OH.  The responsibilities include:

• Key contact with client, managing the start up and regulatory submission process for clinical trials
• Development of project specific regulatory documents – including informed consent
• Interaction with clients, US Central IRBs, sites and international associates
• Manage a team of Regulatory Submissions Coordinators

• 3-5 years of experience in pharmaceutical research trials (pharma or CRO)
• Experience and knowledge as a CRA or Regulatory associate in the start up process for clinical trials
• Ability to manage project teams
• A Bachelor's degree in a relevant field

 

  

Benefits:

• Medpace offers an outstanding compensation and benefits package, including health, dental, PTO, 401(k) with match, and bonuses based on individual and company performance.
• We also offer a 24-hour on-site fitness facility with a personal trainer, as well as a business casual work environment.

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To apply for this position: 

Please send your cover letter and resume to: HR, Medpace, 5375 Medpace Way, Cincinnati, OH 45227; fax to: 513-579-0444; or e-mail to: [Click Here to Email Your Resumé].

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