Oncology Clinical Research Data Coordinator – Part Time

Actalent; New Brunswick (NJ); On-site; USD 34,000 - 45,000; Part time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Transportation benefits

Time Off/Leave (PTO, vacation or sick)

Job summary

Actalent is seeking a part-time Clinical Research Coordinator (Oncology) for on-site work in New Brunswick, NJ. You will support oncology studies by coordinating patient activities, managing data in EDC/EMR systems, and ensuring accurate documentation in line with protocols and regulatory expectations.

Responsibilities include data entry, scheduling, data quality checks, and collaboration with nurses and research staff to maintain study timelines. Prior oncology CRC experience is required.

Qualifications

• At least 2 years of clinical research experience.
• At least 2 years of experience with electronic data capture (EDC) data entry.
• At least 2 years of patient recruitment experience.
• Experience with oncology clinical research.
• Proficiency in pre-screening patients for clinical trials.
• Strong chart review skills using electronic medical records (EMR).
• Experience working as a Clinical Research Coordinator, Registered Nurse, or Licensed Practical Nurse in a research or clinical setting.
• Strong attention to detail and accuracy in data entry and verification.
• Ability to manage multiple tasks such as data entry, scheduling, and query resolution concurrently.
• Effective communication skills for interacting with patients and clinical team members.

Responsibilities

• Perform accurate and timely data entry into electronic data capture (EDC) systems.
• Schedule patient appointments and send reminders to support visit adherence and study timelines.
• Verify data for completeness and accuracy, and resolve data queries in a timely manner.
• Use electronic medical records (EMR) to review patient histories, document study-related information, and track patient progress.
• Support patient recruitment activities by identifying and engaging potential participants.
• Collaborate with clinical staff, including nurses and other research team members, to ensure smooth coordination of study procedures.
• Maintain confidentiality of patient information and follow all applicable clinical research and institutional guidelines.
• Work efficiently in a fast-paced environment while maintaining strong attention to detail and adherence to study protocols.

Skills

Clinical research experience

EDC data entry

Patient recruitment

Oncology clinical research

Pre-screening patients

EMR chart review

CRC/RN/LPN experience in research

Data entry accuracy

multitasking

Communication with clinical team

Tools

EDC systems

EMR systems

Job description

Actalent is seeking a part-time Clinical Research Coordinator (Oncology) for on-site work in New Brunswick, NJ. You will support oncology studies by coordinating patient activities, managing data in EDC/EMR systems, and ensuring accurate documentation in line with protocols and regulatory expectations.

Responsibilities include data entry, scheduling, data quality checks, and collaboration with nurses and research staff to maintain study timelines. Prior oncology CRC experience is required.