Clinical Trials Site Activation Specialist

Medpace

Cincinnati (OH)

On-site

USD 48,000 - 64,000

Full time

14 days+

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Job summary

Medpace is seeking full-time, office-based Project Coordinators to join our Site Activation and Maintenance (SAM) team. This role supports clinical trial management and the study start-up process, working independently and with a team to achieve shared goals.

Responsibilities include coordinating with sites to collect essential documents, maintaining TMF quality, assembling start-up submissions, and tracking timelines across departments.

Qualifications

  • Bachelor's degree required (preferably in Life Sciences).
  • Some healthcare or clinical research experience preferred.
  • Excellent organizational and prioritization skills with strong communication.
  • Proficiency with Microsoft Office applications.
  • Great attention to detail and written/spoken communication.

Responsibilities

  • Communicate with research sites to collect essential documents before screening.
  • Maintain and review trial documents in the TMF.
  • Assemble regulatory start-up submissions, including IRB submissions.
  • Maintain study start-up timelines with internal and external teams.
  • Gain exposure to Oncology/Hematology, Cardiovascular, and Metabolic areas.
  • Provide guidance to team members to ensure regulatory compliance.
  • Review regulations to develop proactive regulatory solutions.
  • Participate in SAM training program modules and mentoring.

Skills

Organizational skills
Prioritization
Communication skills
Attention to detail

Education

Bachelor's degree in Life Sciences or related field

Tools

Microsoft Office

Job description

Medpace is seeking full-time, office-based Project Coordinators to join our Site Activation and Maintenance (SAM) team. This role supports clinical trial management and the study start-up process, working independently and with a team to achieve shared goals.

Responsibilities include coordinating with sites to collect essential documents, maintaining TMF quality, assembling start-up submissions, and tracking timelines across departments.

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