We aspire to meet all of our commitments and provide the best value to our clients. To accomplish our goals, we operate with a team-oriented mentality and enjoy a collaborative environment.

We are reshaping the clinical trial process

Looking for an energetic clinical project coordinator that has DIRECT experience in the clinical research industry.  If interested, please submit your resume to Paige Queen, Senior Vice President, Clinical Operations at pqueen@totalcro.com.

Job Summary:

In this role, the Project Coordinator teams with the assigned Project Manager(s) and has primary responsibility for document management, issue management and project reporting. This is a ‘hands-on’ role that will be responsible for ongoing operational support for existing projects as well as supporting new project implementations, including but not limited to managing and updating project materials, maintaining study files, facilitating IRB submissions and tracking approvals, disseminating regulatory binders to the sites, and maintaining the TMF for the assigned study. Most importantly, the role of the Project Coordinator is to establish and maintain strong site relationships.

Qualifications:

  • BA/BS degree in relevant field required
  • 3+ years of experience performing project coordination in a clinical research related environment
  • Strong competency with MS Office Suite
  • Must be able to perform well with minimal direction in a highly-dynamic, timeline-driven environment