CLINICAL RESEARCH REGULATORY COORDINATOR - CNI

COOPER PEDIATRICS; Camden (NJ); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Health, dental, vision insurance

Life and disability insurance

Retirement plans

Professional development opportunities

Job summary

COOPER PEDIATRICS in Camden, New Jersey is seeking a Clinical Research Regulatory Coordinator to ensure regulatory compliance and accurate documentation for clinical research. The role includes managing submissions and facilitating communication among stakeholders.

Candidates should possess a Bachelor’s Degree, with a Master’s preferred, and have 3-5 years of relevant experience.

Qualifications

• 3-5 years of experience required.

Responsibilities

• Ensure regulatory compliance for all clinical research studies.
• Manage submissions to regulatory agencies and maintain documentation.
• Facilitate communication among Investigators, sponsors, and institutional offices.

Education

Bachelor’s Degree

Masters preferred

Job description

About us

At Cooper University Health Care, our commitment to providing extraordinary health care begins with our team. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. We have a commitment to our employees to provide competitive rates and compensation programs. Cooper offers full and part-time employees a comprehensive benefits program, including health, dental, vision, life, disability, and retirement. We also provide attractive working conditions and opportunities for career growth through professional development.

Discover why Cooper University Health Care is the employer of choice in South Jersey.

Short Description

• The Clinical Research Regulatory Coordinator ensures regulatory compliance and accurate documentation for all clinical research studies conducted at Cooper University Health Care.
• This role supports study startup, maintenance, and closeout by managing submissions to regulatory agencies, maintaining Investigator and staff documentation, and facilitating communication among Investigators, sponsors, and institutional offices.

Experience Required

3-5 years required.

Education Requirements

Bachelor’s Degree required. Masters preferred.