Data Coordinator

Insight Global; Hackensack (NJ); On-site; USD 42,000 - 65,000; Full time

Job summary

Insight Global is seeking a Data Coordinator for a Cancer Research project in Hackensack, NJ. The role involves accurate data entry from EMR into EDC systems, ensuring data quality and protocol compliance, and promptly resolving data queries.

Responsibilities include preparing and maintaining laboratory kits, processing and shipping human specimens, and supporting monitoring visits and site documentation in accordance with Good Clinical Practice.

Qualifications

• At least 1 year of data/research experience.
• Bachelor's degree in health science preferred.
• Exposure to medical terminology.
• Experience with Google Sheets or similar spreadsheets.
• Excellent verbal and written communication.
• Detail-oriented with strong organizational and analytical skills.

Responsibilities

• Enter clinical research data from EMR into EDC with accuracy and timeliness.
• Ensure data quality and protocol compliance; resolve data queries promptly.
• Prepare and maintain laboratory kits; process and ship human specimens per protocol.
• Support monitoring visits from site initiation to close-out; maintain study documentation.

Skills

Data/Research experience

Medical terminology

Communication skills

Detail oriented

Education

Bachelor's degree in Health science

Tools

Google Sheets

Job description

• At least 1 year of experience Data/Research experience
• Bachelors Degree - Health science preferred
• Pervious exposure to medical terminology
• Prior experience with Google Sheet or similar spreadsheet experience
• Excellent verbal and written communication skills
• Detail orientated with strong organizational and analytical skills

Plusses

Day to Day:

Insight Global is looking for a Data Coordinator for our Cancer Research client in Hackensack, NJ. The role is responsible for accurate and timely entry of clinical research data from EMR systems into EDC platforms, ensuring data quality, protocol compliance, and prompt resolution of queries. Responsibilities include preparing and maintaining laboratory kits, processing and shipping human specimens according to study protocols and regulatory requirements, and supporting all phases of monitoring visits, including site initiation, routine monitoring, and close-out. The position works closely with investigators, research staff, sponsors, and CROs to support study conduct, maintain documentation, and ensure adherence to Good Clinical Practice and institutional policies.