Senior Clinical Research Coordinator: Protocol & Study Lead

tulanectsi; New Orleans, Northern (LA, KY); Hybrid; USD 60,000 - 80,000; Full time

Job summary

Tulane University is seeking a Clinical Research Coordinator III to coordinate and conduct all aspects of a clinical study with minimal supervision. The role requires deep knowledge of protocol requirements and good clinical practices under federal regulations.

You will serve as the primary resource for the protocol, liaising between patients, investigators, collaborators, and the IRB, and assist with protocol development and SOPs.

Qualifications

• Bachelor’s Degree or RN with current state licensure at the time of hire.
• LPN with current state licensure at the time of hire.
• Master’s Degree in a related field and one year of related work experience.
• Certification as a CCRC or CCRP is strongly desired.
• Supervisory experience is preferred.

Responsibilities

• Coordinate and conduct all aspects of a clinical study with minimal supervision.
• Assist investigators to develop study protocol and manuals of procedures.
• Act as liaison between patient, investigator, collaborators, and IRB.
• Screen, enroll and follow study participants, conduct data collection and entry.
• Maintain data and source documentation, adverse event reporting, and IRB files.

Education

Bachelor’s Degree or RN

LPN with licensure

Master’s Degree in related field

Job description

Tulane University is seeking a Clinical Research Coordinator III to coordinate and conduct all aspects of a clinical study with minimal supervision. The role requires deep knowledge of protocol requirements and good clinical practices under federal regulations.

You will serve as the primary resource for the protocol, liaising between patients, investigators, collaborators, and the IRB, and assist with protocol development and SOPs.