Remote Clinical Trials Project Support Specialist

Precision for Medicine

United States

Remote

USD 52,000 - 78,000

Full time

14 days+
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Job summary

Precision for Medicine seeks a Project Support Specialist to join the project team and provide cross-functional support to ensure efficient study management. The role supports timelines, meetings, CTMS data, training, and document control across various trial activities.

Minimum 4-year college degree with at least 2 years in a similar clinical trial support role and strong Microsoft Office skills are required.

Qualifications

  • 4-year college degree or equivalent experience in business, science or healthcare.
  • Minimum of 2 years of relevant experience as a Clinical Trial Assistant, Clinical Support Specialist or similar role.
  • Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint).

Responsibilities

  • Create and maintain project timelines in MS Project or similar system.
  • Schedule meetings, prepare agendas, take minutes and file them in the Trial Master File.
  • Maintain CTMS data including milestone dates and enrolment projections.
  • Prepare and document study training; manage training records and identify gaps.
  • Establish study-level SharePoint site and manage access for team and sponsors.
  • Create project-specific email boxes and manage access to study systems.
  • Manage user access requests and conduct periodic access reviews.
  • Order study supplies and initial binders and arrange shipping to locations.
  • Maintain study trackers and assist with study reports and updates.

Skills

Communication
Teamwork
Attention to detail
Customer service

Education

Bachelor's degree

Tools

MS Office

Job description

Precision for Medicine seeks a Project Support Specialist to join the project team and provide cross-functional support to ensure efficient study management. The role supports timelines, meetings, CTMS data, training, and document control across various trial activities.

Minimum 4-year college degree with at least 2 years in a similar clinical trial support role and strong Microsoft Office skills are required.

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