Senior Clinical Research Coordinator - Protocol & Study Lead

Tulane University; New Orleans (LA); On-site; USD 65,000 - 90,000; Full time

Job summary

Tulane University is seeking a Clinical Research Coordinator III to coordinate all aspects of a clinical study with minimal supervision. The role requires in-depth protocol knowledge and GMP practices to support investigators and maintain regulatory files.

The position involves screen/enroll of participants, data collection, and noninvasive testing, while serving as a primary resource for protocol and liaison among patients, investigators, and IRB teams, ensuring compliance and quality across

Qualifications

• Bachelor’s Degree or RN with current state licensure at the time of hire and two (2) years of related work experience.
• LPN with current state licensure at the time of hire and five (5) years of related work experience.
• Master’s Degree in a related field and one (1) year of related work experience.

Responsibilities

• Coordinate and conduct all aspects of a clinical study with minimal supervision.
• Act as liaison between patient, investigator, collaborators, and IRB; ensure protocol adherence.
• Screen, enroll and follow study participants; conduct data collection and entry per protocol.
• Keep data and source documentation, report adverse events, and maintain IRB regulatory files.
• Assist investigators in developing study protocol and manuals of procedures; provide protocol guidance.

Skills

Good clinical practices

Study coordination

IRB liaison

Data collection and entry

Noninvasive testing

Education

Bachelor’s Degree

RN licensure

LPN licensure

Master’s Degree

Job description

Tulane University is seeking a Clinical Research Coordinator III to coordinate all aspects of a clinical study with minimal supervision. The role requires in-depth protocol knowledge and GMP practices to support investigators and maintain regulatory files.

The position involves screen/enroll of participants, data collection, and noninvasive testing, while serving as a primary resource for protocol and liaison among patients, investigators, and IRB teams, ensuring compliance and quality across