Clinical Research Coordinator I

Tulane University • Bogalusa, LA

7h • Hybrid

About The Position

The Clinical Research Coordinator (CRC) will coordinate multiple projects that are on-going in the Bogalusa Heart Study (BHS) Clinic located primarily in Bogalusa, Louisiana. This individual will work with the Principal Investigator(s) to coordinate the conduct of studies between the filed site in Bogalusa and the central administration of the study in New Orleans. Therefore, regular travel between Bogalusa and New Orleans will be a requirement. In addition, the CRC will coordinate meetings of the BHS Steering Committee, other BHS investigators, collaborators from other universities, and take minutes. The CRC will provide recruitment reports, enrollment reports, and other study reports to the investigators to monitor the conduct of the study. They will be responsible for developing and maintaining documentation and update of protocols and manuals of operation, and regulatory documentation as needed for the on-going studies.

Requirements

• Bachelor’s degree or RN with current LA licensure at the time of hire
• Two years professional clinical research work experience, or in lieu of that an advanced degree such as Masters degree in Clinical Research, Clinical Investigation, Public Health or related field.

Nice To Haves

• Experience with research coordination and teams
• Applied IRB experience
• Experience working with clinical and community partners when doing research
• Competent with technology (MS Office Suite, including Excel and PowerPoint; Outlook; Zoom)
• Ability to do literature review
• Ability to conduct basic statistical analysis
• Familiarity with database software and programming (REDCap; SQL; others)

Responsibilities

• Coordinate multiple ongoing projects in the Bogalusa Heart Study (BHS) Clinic.
• Coordinate study conduct between the Bogalusa field site and New Orleans central administration.
• Coordinate meetings of the BHS Steering Committee, other BHS investigators, and collaborators.
• Take minutes for meetings.
• Provide recruitment reports, enrollment reports, and other study reports to investigators.
• Develop and maintain documentation and updates of protocols and manuals of operation.
• Maintain regulatory documentation as needed for ongoing studies.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level