CLINICAL TRIALS COORDINATOR 1 or 2

LSU; New Orleans (LA); On-site; USD 52,000 - 76,000; Full time

Job summary

LSU Health Sciences Center, Department of Orthopaedic Surgery in New Orleans, seeks a Research Clinical Trial Coordinator 1 or 2 to support regulatory activities, IRB submissions, and enrollment in federally funded orthopedic studies.

You will work with Dr. Jessica Rivera to screen, consent, and enroll participants, handling regulatory paperwork and study coordination in a hospital/academic setting.

Qualifications

• Bachelor's degree required in Physical Sciences, Healthcare/Public Health or related field.
• Certified Clinical Trial Coordinator credentials (CTRC/CCRP) for CTC2 preferred.
• CTC1: 1 year experience; CTC2: 3 years experience in clinical trials.

Responsibilities

• Assist with regulatory paperwork and IRB submissions.
• Screen potential participants for eligibility.
• Obtain informed consent from participants.
• Enroll eligible participants into clinical studies.

Skills

Clinical trial coordination

Recruitment

IRB submissions

Informed consent

Regulatory paperwork

Education

Bachelor's degree in Physical Sciences/Healthcare/Public Health

Job description

Position Overview

LSU Health Sciences Center, Department of Orthopaedic Surgery in New Orleans is seeking a research Clinical Trial Coordinator 1 or 2. This position will work specifically on clinical research in the Department of Orthopaedic Surgery. The CTC will work directly with Dr. Jessica Rivera. The Department has multiple federally funded studies that require a dedicated CTC to assist with regulatory paperwork, IRB submission, screening of possible patients, consenting, and enrollment into the study.

Minimum Qualifications

Minimum Qualifications Required Education: Bachelor's Required Field of Study: Physical Sciences (biology, chemistry, physics, etc), Healthcare/Public Health or related field Certifications or Licenses Required: Clinical Trial Coordinator 2: CCRC/CCRP or related Clinical Research Certification Number of years required to perform the job: Clinical Trials Coordinator 1: 1 year; Clinical Trials Coordinator 2: 3 years Type of experience required to perform the job: Experience with recruitment or in other public health related work; Research or clinical experience in a hospital/clinic/academic setting Substitution: At the CTC 1 or 2 level, an LPN and 2 additional years may substitute for the Bachelors. At the CTC 2 level, one additional year of Clinical Trials experience may substitute for the CCRC/CCRP at the department's discretion. AT ANY LEVEL, a Masters or MD degree can substitute for one year of experience.