Clinical Trials Coordinator: Impactful Research & Compliance

Hackensack Meridian Health; 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

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