Clinical Research Coordinator: Lead Trials & Compliance

Hackensack Meridian Health; Hackensack (NJ); On-site; USD 75,000 - 92,000; Full time

Job summary

Hackensack Meridian Health is seeking a dedicated Clinical Research Coordinator in New Jersey to coordinate and oversee clinical trial operations, ensuring compliance with local, state, and federal regulations. The role requires a BA/BS in science or healthcare and 2+ years of clinical research experience.

Strong attention to detail and the ability to work independently or in a team are essential. Familiarity with budgeting, data management, and subject enrollment is preferred.

Qualifications

• BA/BS diploma/degree in science or healthcare field.
• Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field of clinical research.
• Strong attention to detail and customer service focus.
• Ability to work independently, or in a team, and handle multiple deadline driven tasks in a dynamic environment is essential.
• Excellent organizational, presentation, documentation and interpersonal skills.

Responsibilities

• Coordinate and oversee clinical operations of assigned trials in accordance with regulatory requirements.
• Ensure informed consent is properly obtained and documented.
• Review budgets and study protocols for feasibility and cost implications.
• Schedule tests, visits, and regulatory activities as required.
• Maintain essential trial records and communicate with sponsors and IRB as needed.

Skills

Attention to detail

Communication skills

Independent or team work

Education

BA/BS diploma/degree in science or healthcare field

SOCRA-Certified Clinical Research Professional (CCRP) and/or CCR A/CCRC

Job description

Hackensack Meridian Health is seeking a dedicated Clinical Research Coordinator in New Jersey to coordinate and oversee clinical trial operations, ensuring compliance with local, state, and federal regulations. The role requires a BA/BS in science or healthcare and 2+ years of clinical research experience.

Strong attention to detail and the ability to work independently or in a team are essential. Familiarity with budgeting, data management, and subject enrollment is preferred.