Data Coordinator

Join to apply for the Data Coordinator role at The START Center for Cancer Research
.

Location:

629 Cranbury Rd., East Brunswick, NJ 08816 (onsite). Hourly rate: $23–$25 per hour, may vary based on market, experience, and skills.

The START Center for Cancer Research (“START”) is the world’s largest early‑phase site network, fully dedicated to oncology clinical research. It has completed over 1,300 studies and operates in the United States and Europe, accelerating the development of new anticancer drugs and improving patient outcomes.

• Collect, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case report forms (CRFs); correct and resolve queries for assigned investigational drug studies.
• Receive and request patient records/data from the study team to complete CRFs.
• Review patient data for completeness and accuracy.
• Coordinate and schedule monitor visits, including exit meetings to review data or queries.
• Identify lab facilities used for assigned studies and communicate with Regulatory Affairs staff so lab certifications can be requested.
• Use protocols as guides for study activities.
• Ensure data entry remains current for all assigned studies.
• Attend meetings as required (site initiation, monitor exit, close‑out, audit preparation).
• Be available on‑site during audits.
• Communicate with accounts receivable staff regarding submitted data.

• Bachelor’s degree or equivalent experience.
• Knowledge and training in general office administration skills, including computer applications and filing systems.

• Ability to accurately perform data review and CRF completion independently.
• Familiarity with medical terminology.
• Demonstrated clinical research knowledge, such as possession of CCRP or CCRC credentials.

• Travel required up to 10% of the time.
• Ability to sit for extended periods.
• Typing and computer use for extended periods.

• Comprehensive health coverage: medical, dental, and vision insurance.
• Robust retirement planning: 401(k) plan with employer matching.
• Life and disability insurance.
• Health savings and flexible spending accounts.
• Paid time off, flexible schedule, and remote work options.
• Collaborative, creative environment fostering growth and innovation.

Deeply rooted in community oncology centers worldwide, START provides access to specialized preclinical and early‑phase clinical trials of novel anti‑cancer agents. Its eight clinical trial sites have conducted more than a thousand early‑phase trials, including 43 therapies approved by the FDA/EMA.

We are an equal‑opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.