Clinical Data Coordinator

About the Company

The START Center for Cancer Research is a global leader in early-phase oncology research, operating the largest dedicated site network of its kind. Its mission is to expand access to advanced clinical trials and help bring new cancer therapies to patients across the United States and Europe.

Role Overview

The organization is looking for a detail-oriented Clinical Data Coordinator to support investigational drug studies by collecting, entering, transcribing, and submitting clinical data accurately and on time.

Compensation and Schedule

This role offers an hourly pay rate of $24.00 to $27.00, depending on experience, qualifications, and internal equity. Team members in this position may also qualify for an annual bonus of up to 10% of base earnings.

The standard work schedule is Monday through Friday, 8:00 am to 5:00 pm EST.

The position is based at 629 Cranbury Rd., Suite 102, East Brunswick, NJ 08816.

Key Duties

• Handle the collection, transcription, entry, and submission of clinical data in paper and electronic case report forms, including corrections and query follow-up for assigned investigational drug studies.
• Obtain patient records and other study data from the study team when needed to complete case report forms.
• Check patient information for accuracy and completeness across assigned studies.
• Arrange and coordinate monitor visits, including exit discussions to review queries or data issues.
• Determine which laboratory facilities are being used for each study and relay that information to Regulatory Affairs so lab certifications can be requested for the study file.
• Use study protocols as the working guide for day-to-day study activities.
• Keep data entry up to date for all assigned studies.
• Participate in required study meetings such as site initiation, monitor exit, close-out, and audit preparation sessions.
• Communicate with accounts receivable staff as needed regarding submitted data.

Education and Experience

• A bachelor’s degree is preferred, although equivalent work experience may be accepted in place of the degree.
• Previous experience in a clinical research organization is required.

Preferred Qualifications

• Credentials such as CCRP or CCRC are strongly preferred and indicate added clinical research expertise.

Benefits and Perks

• Medical, dental, and vision coverage are included.
• A 401(k) retirement plan with employer matching is available.
• Life and disability insurance are provided.
• Health savings accounts and flexible spending accounts are offered.
• Paid time off, a flexible schedule, and remote work options support work-life balance.
• The company emphasizes a collaborative and creative workplace where employees can learn, grow, and contribute to decisions, planning, and culture.

About the Employer

The START Center for Cancer Research focuses on community-based oncology centers and specialized preclinical and early-phase clinical trials of new anti-cancer treatments. Its sites have completed more than a thousand early-phase trials, including work tied to 43 FDA-approved therapies. The organization operates the world’s largest network of principal investigators across eight clinical trial sites.

Equal Opportunity Statement

The employer is committed to equal opportunity and welcomes applicants from all backgrounds, without discrimination based on 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 legally protected status.