Clinical Research Coordinator I

Tulane University

Bogalusa (LA)

On-site

USD 52,000 - 78,000

Full time

2 days ago

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Job summary

Tulane University in Bogalusa, LA seeks a Clinical Research Coordinator to oversee multiple BHS studies, coordinating with the Principal Investigators and the central study team in New Orleans. The role requires regular travel between Bogalusa and New Orleans to ensure smooth conduct and documentation.

Responsibilities include developing protocol and regulatory materials, generating recruitment and enrollment reports, taking meeting minutes, and maintaining protocol manuals.

Qualifications

Bachelor’s degree or RN with LA licensure at hire.
Two years professional clinical research experience or advanced degree in related field.

Responsibilities

Coordinate multiple studies between Bogalusa site and central administration in New Orleans.
Coordinate meetings of the BHS Steering Committee and other investigators; take minutes.

Skills

Team coordination

Literature review

Statistics basics

Communication

Project management

Education

Bachelor’s degree or RN with LA licensure

Advanced degree in Clinical Research/Investigation/Public Health

Tools

MS Office (Excel, PowerPoint, Outlook, Zoom)

REDCap

SQL

Job description

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.

Qualifications

Minimum Qualification:

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 and advanced degree such as Masters degree in Clinical Research, Clinical Investigation, Public Health or related field.

Preferred Qualification:

Experience with research coordination and teams
Applied IRB experience and 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 and conduct basic statistical analysis
Familiarity with database software and programming (REDCap; SQL; others)

About Us

Tulane University is an equal opportunity educator and employer committed to providing an education and employment environment free of unlawful discrimination, harassment, and retaliation. Legally protected demographic classifications (such as a person’s race, color, religion, age, sex, national origin, shared ancestry, disability, genetics, veteran status, or any other characteristic protected by federal, state, or local laws) are not relied upon as an eligibility, selection or participation criteria for Tulane’s employment or educational programs or activities.

Tulane University is responsible for providing reasonable accommodations to individuals with disabilities throughout the applicant screening process. If you need assistance in completing an application or during any phase of the interview process, please contact the Office of Human Resources by phone at 504-865-4748 or by email at hr@tulane.edu .

Job Info