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Tulane University · 1 month ago

Clinical Research Coordinator II

New Orleans, LA

Full-time

Onsite

Entry, Mid Level

1+ years exp

Tulane University is seeking a Clinical Research Coordinator II to manage all aspects of conducting clinical trials. The role involves acting as a liaison between various stakeholders and ensuring protocol compliance while maintaining regulatory files.

EducationHigher EducationMedical

Responsibilities

Manage all aspects of conducting clinical trials

Act as a liaison between the patient, investigator, Institutional Review Board and sponsor

Screen, enroll and follow study patients, ensuring protocol compliance and close patient monitoring

Maintain all data and source documentation, adverse event reporting and maintenance of complete regulatory files

Qualification

Clinical research practiceIRB submission processCITI training certificatesPatient interactionRegulatory compliance

Required

Knowledge of good clinical research practice is required

Must be able to interact well with patients and the general public

Ability to acquire and maintain all required CITI training certificates

Ability to acquire and maintain credentialing at all required institutions: Tulane Medical Center, Veterans Administration Hospital/New Orleans, LA and University Medical Center

Bachelor's degree or RN with current Louisiana state licensure at the time of hire and one (1) year of related work experience

LPN with current Louisiana state licensure at the time of hire and four (4) years of related work experience

Preferred

Knowledge of IRB submission process and requirements

Knowledge of good clinical practices as set forth by federal regulations

Company

Tulane University

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A member of the prestigious Association of American Universities, Tulane University is consistently ranked among the top 50 universities in the nation.

Founded in 1834

New Orleans, Louisiana, USA

1001-5000 employees