Entry-Level Clinical Start-Up Coordinator: Launch Your Career

Medpace

Cincinnati (OH)

On-site

USD 45,000 - 65,000

Full time

14 days+

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Benefits offered by this job

Health benefits
Retirement plan
Paid time off
WFH flexibility

Job summary

Medpace is seeking full-time, office-based Study Start-Up Coordinators to join our Regulatory Submissions team in Cincinnati, OH. This entry-level position offers a robust training program to build a foundation in clinical research and grow your career.

You will work to collect essential documents, review TMF files, submit regulatory start-up documentation, and maintain study timelines through collaboration with the team.

Qualifications

  • Bachelor's degree required; Life Sciences preferred.
  • Some office experience is preferred.
  • Excellent organizational and prioritization skills.
  • Knowledge of Microsoft Office;
  • Great attention to detail and excellent oral and written communication skills.

Responsibilities

  • Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial;
  • Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);
  • Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards); and
  • Maintain timelines for study start-up through internal team collaboration.

Skills

Organizational skills
Prioritization
Attention to detail
Communication skills

Education

Bachelor's degree in Life Sciences

Tools

Microsoft Office

Job description

Medpace is seeking full-time, office-based Study Start-Up Coordinators to join our Regulatory Submissions team in Cincinnati, OH. This entry-level position offers a robust training program to build a foundation in clinical research and grow your career.

You will work to collect essential documents, review TMF files, submit regulatory start-up documentation, and maintain study timelines through collaboration with the team.

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