Clinical Trials Coordinator & Study Lead

Prolerity Clinical Research, Inc.; Metairie (LA); On-site; USD 52,000 - 75,000; Full time

Job summary

Prolerity Clinical Research, Inc. is seeking a Clinical Research Coordinator (CRC) who will oversee daily operational activities of assigned clinical studies, working with investigators, staff, sponsors, and CROs to ensure compliance with protocols and regulatory standards.

The CRC will own study coordination, documentation, data management, and sponsor communication from startup through close-out, plus recruitment support, site visits, data entry into EDC, adverse event reporting, and

Qualifications

• Bachelor’s degree in a related field.
• Minimum of two (2) years of clinical research or clinical trial management experience.
• Preferred credentials: Medical certification or licensure (e.g., MS, LPN, RN).
• Phlebotomy experience with blood draws and handling biological specimens.

Responsibilities

• Organize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out.
• Support study start-up activities including feasibility, regulatory submissions, and site activation.
• Attend investigator meetings, site initiation visits, and other study-related meetings.
• Manage visit schedules and coordinate study-related activities across clinical teams.
• Collaborate with recruitment teams to support participant screening and enrollment.
• Conduct informed consent discussions with participants and document consent.
• Monitor subjects per protocol; report adverse events with PI and staff.
• Enter study data into EDC and maintain source documentation and regulatory files.
• Collect, process, package, and ship study specimens; perform phlebotomy when trained.
• Ensure SOPs, GCP, and regulatory compliance; support audits and quality assurance.
• Serve as primary sponsor/CRO communications contact; support outreach and updates.

Skills

Leadership

Organization

Attention to detail

Independent work

Time management

Office equipment

Confidentiality

Education

Bachelor's degree

Tools

EDC systems

Job description

Prolerity Clinical Research, Inc. is seeking a Clinical Research Coordinator (CRC) who will oversee daily operational activities of assigned clinical studies, working with investigators, staff, sponsors, and CROs to ensure compliance with protocols and regulatory standards.

The CRC will own study coordination, documentation, data management, and sponsor communication from startup through close-out, plus recruitment support, site visits, data entry into EDC, adverse event reporting, and