Clinical Research Coordinator

HACKENSACK UNIVERSITY MED CNTR; Hackensack (NJ); On-site; USD 70,000 - 95,000; Full time

Job summary

Hackensack Meridian Health seeks a Clinical Research Coordinator to coordinate and oversee clinical operations for assigned trials, ensuring compliance with local, state, and federal regulations and SOPs. The role reports to the principal investigator and requires a science/healthcare degree and clinical research experience.

Ideal candidates have strong organizational, communication, and data management skills, plus proficiency in MS Office or Google Suite and a detail-oriented, patient-focused

Qualifications

• Bachelor's degree in science or healthcare is required.
• 2+ years as Senior Clinical Data Coordinator or Senior Regulatory Specialist, or 4+ years in clinical research.
• Strong attention to detail and customer service focus.
• Ability to work independently or in a team under deadlines in a dynamic environment.
• Excellent organizational, presentation, documentation and interpersonal skills.
• Excellent written and verbal communication skills.
• Proficient with Microsoft Office and Google Suite.

Responsibilities

• Coordinate and oversee clinical operations of all assigned trials.
• Assess, plan, implement, and ensure compliant study conduct per SOPs and regulations.
• Work under the supervision of the principal investigator.

Skills

Attention to detail

Customer service

Independent work

Team collaboration

Organizational skills

Presentation skills

Documentation

Interpersonal skills

Written and verbal communication

Clinical research experience

Proficient with MS Office/Google Suite

Education

BA/BS in science or healthcare

Education on human subject research and GCP

Tools

Microsoft Office

Google Suite

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).