Clinical Research Coordinator
IQVIA
full-time
Posted on:
Location Type: Office
Location: Kenner • Louisiana • 🇺🇸 United States
Visit company websiteJob Level
Mid-LevelSenior
Tech Stack
Google Cloud Platform
About the role
- Coordinate clinical research studies conducted by a supervising principle investigator.
- Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved
- Obtains informed consent of research subjects
- Develops strong working relationships and maintain effective communication with study team members
- Completes all protocol related training
- Performs patient/research participant scheduling
- Collects patient/research participant history
- Collects and maintains source documentation
- Manages inventory and administers test articles/investigational product to participants
- Performs data entry and query resolution
- Supports the collection and review of required essential study documents and reports.
- Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging, and laboratory handling manuals, etc.)
- Adheres to an IRB approved protocol
- Supports the safety of research subjects, report adverse events
- Coordinates protocol related research procedures, study visits, and follow-up
- Facilitates pre-study, site qualification, study initiation, monitoring visits, and study close out activities
- Collects, processes and ships laboratory specimens
- May be asked to perform special project responsibilities and travel to other clinic locations, within the area, when needs arise
- Complies with Avacare and Sponsor policies, standard operating procedures (SOPs) and guidelines
- Performs other duties as assigned
Requirements
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
- Clinical Research Coordinator experience within a similar setting preferred
- Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc.
- Knowledge and experience of site operations and the drug development process
- Effective communication
- Computer proficiency in use of Microsoft Word, Excel
Benefits
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical research coordinationpatient recruitment strategiesinformed consentdata entryquery resolutionphlebotomyEKGvital signs monitoringsource documentationlaboratory specimen processing
Soft skills
effective communicationrelationship buildingorganizational skillsteam collaborationproblem-solving
Certifications
GCP certificationICH certification