Clinical Trials Coordinator - Study Ops & Compliance Lead

Prolerity Clinical Research, Inc.; Marrero, Northern (LA, KY); Hybrid; USD 52,000 - 76,000; Full time

Job summary

Prolerity Clinical Research, Inc. is seeking a Clinical Research Coordinator (CRC) to manage daily operations of assigned clinical trials, working with investigators, staff, sponsors, and CROs to ensure compliant execution from start-up to close-out.

The role emphasizes study coordination, data management, participant consent, monitoring, and documentation in EDC systems, with a focus on regulatory compliance, Quality Assurance, and timely communication with sponsors.

Qualifications

• Bachelor’s degree in a related field required.
• Minimum of 2 years in clinical research or trial management.
• Medical certification or licensure preferred (MS, LPN, RN).
• Phlebotomy experience required.

Responsibilities

• Oversee and manage daily operational activities of assigned trials.
• Coordinate start-up activities including feasibility, regulatory submissions, and site activation.
• Attend investigator meetings and site initiation visits.
• Monitor subjects and report adverse events in collaboration with PI.

Skills

Leadership

Communication

Organizational skills

Attention to detail

Regulatory compliance

Multitasking

Confidentiality

Time management

Phlebotomy

Education

Bachelor's degree in a related field

Tools

EDC systems

CRF management software

Microsoft Office

Job description

Prolerity Clinical Research, Inc. is seeking a Clinical Research Coordinator (CRC) to manage daily operations of assigned clinical trials, working with investigators, staff, sponsors, and CROs to ensure compliant execution from start-up to close-out.

The role emphasizes study coordination, data management, participant consent, monitoring, and documentation in EDC systems, with a focus on regulatory compliance, Quality Assurance, and timely communication with sponsors.