Senior Clinical Data Coordinator – Onsite Data Lead

Hackensack Meridian Health; Paramus (NJ); On-site; USD 70,000 - 80,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Paid leave

Tuition reimbursement

Retirement benefits

Job summary

Hackensack Meridian Health is seeking a Senior Clinical Data Coordinator to oversee data management for clinical studies, ensure data integrity, and manage queries. This role requires on-site work in Paramus, NJ five days a week, and close collaboration with investigators, sponsors, and IRB.

The position emphasizes onboarding, data quality, regulatory compliance, and timely data submissions across study teams while partnering with sponsors and site personnel.

Qualifications

• BA/BS in science or healthcare field or equivalent experience (4+ years with HS/GED).
• Strong attention to detail and customer service focus.
• Ability to work independently, or in a team, with multiple deadlines.
• Excellent organizational, presentation, documentation and interpersonal skills.
• Excellent written and verbal communication skills.
• Proficient with Microsoft Office and Google Suite.

Responsibilities

• Onboards newly hired research personnel and provides onboarding training materials for data team members.
• Develops data compliance processes and procedures as needed.
• Ensures electronic databases contain accurate, complete patient data and reviews source documents.

Skills

Attention to detail

Customer service

Independent / Team work

Organizational skills

Written and verbal communication

MS Office / Google Suite

Education

BA/BS in science or healthcare

4+ years of related experience with HS/GED

Tools

MS Office & Google Suite

Job description

Hackensack Meridian Health is seeking a Senior Clinical Data Coordinator to oversee data management for clinical studies, ensure data integrity, and manage queries. This role requires on-site work in Paramus, NJ five days a week, and close collaboration with investigators, sponsors, and IRB.

The position emphasizes onboarding, data quality, regulatory compliance, and timely data submissions across study teams while partnering with sponsors and site personnel.