Regulatory Submissions (Study Start-up) Manager
Medpace | Cincinnati, OH (map it!Map it!) | 8/7/2014
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JOB DESCRIPTION

DESCRIPTION OF JOB DUTIES

  • Efficiently manage and successfully execute all aspects of global start-up according to Sponsor specifications;
  • Perform quality checks on submission documents and site essential documents;
  • Interact with US central IRBs, sites, and international associates;
  • Prepare and approve informed consent forms;
  • Review pertinent regulations to develop proactive solutions to start-up issues and challenges; and
  • Present during bid defenses, general capabilities meetings, and audits.

JOB REQUIREMENTS

QUALIFICATIONS/REQUIREMENTS

  • More than 5 years of experience in clinical research, preferably with a CRO. Experience may include CRA or project management experience;
  • Strong oral and written communication skills.

Travel: Minimal

WHAT TO EXPECT NEXT

We look forward to receiving your application.  A member of our recruitment team will review your qualifications. If interested, you will be contacted for an interview.



EO/AA Employer M/F/Disability/Vets

JOB SNAPSHOT

Employment Type: Full-Time
Base Pay: N/A
Other Pay: N/A
Industry: Healthcare - Health Services
Education: Not Specified
Experience: Not Specified
Manages Others: Yes
Relocation: Not Specified
Required Travel: Not Specified
Job ID: RSM_Cincinnati
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COMPANY OVERVIEW
MedPace

Finding work that is challenging, having the tools and training to succeed, being rewarded and provided opportunities to grow professionally are just a few reasons talented individuals join the Medpace team. With our global presence in a rapidly growing industry, Medpace has quickly become a leader providing ample opportunity for employee growth and development. Our employees define how we work and give us a competitive advantage.

EO/AA Employer M/F/Disability/Vets Learn More...

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