Clinical Trials Coordinator- Virtual req61366 in Raleigh, NC at Quest Diagnostics

Date Posted: 2/18/2021

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    5510 Six Forks Road
    Raleigh, NC
  • Job Type:
  • Experience:
    Not Specified
  • Date Posted:
    2/18/2021
  • Job ID:
    req61366

Job Description

Clinical Trails Coordinator- Virtual - Monday to Friday

Temporary role with possibility of permanent placement.

 Clinical Trials Coordinator – the role:

The Clinical Trials Coordinator will assist Contract Research management in all responsibilities related to clinical trials. This requires an awareness of various ongoing clinical trials and their different requirements. This professional will handle the majority of the day-to-day duties related to the clinical trial projects.


The Clinical Trials Coordinator will work with Contract Research management staff on the drafting, reviewing, or revising of study project SOWs, SOPs, forms and templates. This professional will assist in accessioning and tracking study specimens; assemble and send out shipping kits; manage correspondence with clients and track send back of materials. The Clinical Trials Coordinator will also participate in QA audits and responses.

Job responsibilities:
Assist Project Managers in study management duties
Assist in preparing study related documents and SOPs
Assist in tracking and reporting of program metrics for all recruitment campaigns
Assists in development of project timelines
Assists in coordination of internal stakeholders for project kick off and close out activities
Archive study slides an draw data according to SOW
Assist with data entry and/or auditing of data in a manner compliant with SOW
Document all projects at an appropriate level
Participate in meetings, trainings, committees and teleconferences as needed
Participate in GLP Projects in compliance with Testing Protocol and GLP requirements
Support the preparation for site QA audits and assist in the follow up on audit recommendations

 
To qualify, the ideal candidate will have the following skills and experience:
Bachelor’s degree in Biology, Chemistry, or a related science
2+years of experience in a clinical laboratory or CRO
Ability to manage several projects under supervision
Ability to understand and address customer issues and work with management to ensure effective and long-term solutions
Knowledge and application of GCP, FDA, and ICH guidelines.
Demonstrated success with building trust and strong relationships with others; follows through on commitments
Demonstrated proficiency with Microsoft Office suite of products, particularly Power Point, Word and Excel.  

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