Clinical Project Associate - new job in North Chesterfield, US

Clinical Project Associate
  • Competitive
  • Permanent
  • North Chesterfield VA, US North Chesterfield CHESTERFIELD US
Job Ref: JO000132390
Sector: Clinical
Sub-sector: Clinical
Date Added: 01 August 2022

At SRG, we create meaningful connections that empower individuals and businesses to shape tomorrow’s world.

Working as part of the SRG team, the Clinical Project Associate has responsibility for clinical operations support of studies spanning study start up to study close out/reporting/filing.


The responsibilities of this job include, but are not limited to, the following:

  • Works with internal department (Clinical Project Manager, Clinical Program Lead, or Clinical Study Team) and CROs/Vendors to support essential daily clinical trial activities, including but not limited to meeting minutes, reviewing invoices, tracking budgets, and contract management.
  • Ensures high quality TMF setup, management, and oversight
  • Contributes to the TMF management plan, study specific preparation of documents in the system, management of cross functional periodic reviews, follows up on open record management queries and ensures their full resolution, etc.)
  • Monitors, identifies, and reports quality problems and record management work practices to Clinical Project Manager
  • Liaises with internal and external teams to ensure completeness and quality of documents
  • Monitors, identifies, and reports quality problems and record management work practices to TMF management
  • Can perform essential document review and tracking of documentation

Here’s What You’ll Bring to the Table:

  • Bachelor’s degree and Minimum 3 Years of clinical research related experience, or Associate’s degree + Minimum of 6 years clinical research related experience
  • Experience as an in-house clinical research associate, TMF specialist, or a field clinical research associate is a plus) G
  • lobal clinical trial/study support experience preferred, but US clinical trial experience is required
  • Working knowledge of Good Clinical Practices, monitoring, clinical and essential regulatory documents/ clinical trial documents
  • Demonstrated study/project support in a matrix environment
  • Strong problem-solving skills
  • Excellent communication skills, both written and verbal

SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.

31/08/2022 12:00:00
USD 0.00 0.00 Hour
Contact Consultant:
Danielle Wilson

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