Clinical Research Coordinator

Hackensack Meridian Health Inc.; Paramus (NJ); On-site; USD 65,000 - 85,000; Full time

Job summary

Hackensack Meridian Health is seeking a Clinical Research Coordinator to coordinate and oversee clinical operations for assigned trials, ensuring compliant conduct under PI supervision. The role demands meticulous attention to regulatory polices, SOPs, and quality assurance.

Ideal candidates will have a BA/BS in science or healthcare, 2–4 years in clinical research roles, and strong written and verbal communication skills, with proficiency in Microsoft Office/Google Suite.

Qualifications

• BA/BS in science or healthcare field.
• Minimum 2 years in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in 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.
• Excellent written and verbal communication skills.
• Proficient computer skills that include Microsoft Office and/or Google Suite platforms.

Responsibilities

• Coordinate and oversee clinical operations of all assigned clinical trials.
• Assist in assessing, planning, implementing and compliant study conduct according to regulatory and institutional SOPs.
• Work under supervision of the principal investigator responsible for the trials.

Skills

Attention to detail

Communication skills

Teamwork

Independent work

Customer service

Microsoft Office / Google Suite

Education

BA/BS in science or healthcare

Tools

Microsoft Office

Google Workspace

Job description

Our team members are the heart of what makes us better.

At Hackensack Meridian Health we help our patients live better, healthier lives — and we help one another to succeed. With a culture rooted in connection and collaboration, our employees are team members. Here, competitive benefits are just the beginning. It’s also about how we support one another and how we show up for our community.

Together, we keep getting better - advancing our mission to transform healthcare and serve as a leader of positive change

The Clinical Research Coordinator is responsible for coordinating and overseeing clinical operations of all assigned clinical trials and participates in assessing, planning, implementing and compliant study conduct according to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures. This role carries out the research and works under the general supervision of the principal investigator responsible for the clinical trial(s) to which is assigned.

Education, Knowledge, Skills and Abilities Required:

• 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.
• Excellent written and verbal communication skills.
• Proficient computer skills that include but are not limited to Microsoft Office and/or Google Suite platforms.

Education, Knowledge, Skills and Abilities Preferred:

• Education on human subject research and GCP.

Licenses and Certifications Preferred:

• SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC).