Senior Cardiology Clinical Research Lead

Cooper University Health Care; Camden (NJ); On-site; USD 56,000 - 96,000; Full time

Job summary

Cooper Norcross Health is seeking a Lead Clinical Research Coordinator for Cardiology in Camden, NJ. The role requires 3–5 years of experience (6–10 preferred) and a Bachelor's degree (Masters preferred). Certification such as CCRC/CCRP is preferred.

The position offers day shifts and a competitive hourly pay range. The CRTL will provide senior operational leadership, guide staff on protocol requirements, documentation, and workflows, and ensure compliant study conduct under GCP and

Qualifications

• Bachelor's Degree required.
• 3-5 years required; 6-10 years preferred.
• CCRC and CCRP preferred.

Responsibilities

• The Clinical Research Team Lead provides senior-level operational leadership and oversight of assigned clinical research studies and serves as the first-line resource for research staff on clinical trial operations, protocol requirements, participant management, documentation, and workflows.
• The LCRC provides guidance, mentorship, and troubleshooting support, resolves routine operational issues, and escalates complex or high-risk matters to the Research Manager or appropriate leadership.
• The role promotes compliant, efficient, and consistent study conduct in accordance with protocols, GCP, regulatory requirements, and institutional policies, while functioning in a supervisory capacity without formal HR or personnel management responsibilities.

Skills

Clinical research leadership

Participant management

Documentation

Regulatory compliance

Study coordination

Education

Bachelor's Degree

Master's degree preferred

Job description

Cooper Norcross Health is seeking a Lead Clinical Research Coordinator for Cardiology in Camden, NJ. The role requires 3–5 years of experience (6–10 preferred) and a Bachelor's degree (Masters preferred). Certification such as CCRC/CCRP is preferred.

The position offers day shifts and a competitive hourly pay range. The CRTL will provide senior operational leadership, guide staff on protocol requirements, documentation, and workflows, and ensure compliant study conduct under GCP and