Clinical Research Coordinator

Hackensack Meridian Health Inc.; Hackensack (NJ); On-site; USD 60,000 - 80,000; Full time

Job summary

Hackensack Meridian Health Inc. is seeking a Clinical Research Coordinator to oversee clinical operations for trials. This role requires a BA/BS degree in science or healthcare, with at least 2 years of experience as a Senior Clinical Data Coordinator or similar.

The coordinator will ensure compliance with regulatory standards and work closely with the principal investigator. Strong organizational and communication skills are essential, along with proficiency in Microsoft Office and Google Suite.

Qualifications

• Minimum 2 years in Senior Data Coordinator or Senior Regulatory Specialist role.
• At least 4 years related experience in clinical research.
• Ability to work independently or in a team in a dynamic environment.

Responsibilities

• Coordinate and oversee clinical operations of assigned clinical trials.
• Participate in assessing, planning and implementing compliant study conduct.
• Work under the general supervision of the principal investigator.

Skills

Attention to detail

Customer service

Organizational skills

Presentation skills

Documentation skills

Interpersonal skills

Written communication

Verbal communication

Microsoft Office

Google Suite

Education

BA/BS in science or healthcare field

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).

If you feel that the above description speaks directly to your strengths and capabilities, then please apply today!