Oncology Clinical Research Coordinator - Part Time

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

Benefits offered by this job

Medical, dental & vision

Critical Illness, Accident, and Hospin

401(k) Retirement Plan

Pre-tax and Roth post-tax contrib

Life Insurance (Voluntary Life & AD&D)

Short and long-term disability

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

Time Off/Leave (PTO, Vacation or Sick)

Job summary

Actalent is seeking a part-time Clinical Research Coordinator (Oncology) based in New Brunswick, NJ. The role focuses on coordinating oncology studies, data management, scheduling, and regulatory adherence in a fast-paced clinical research environment.

You will work with clinical teams to pre-screen patients, verify eligibility, and maintain high-quality data in EMR and EDC systems while ensuring patient confidentiality and protocol compliance.

Qualifications

• Minimum 2 years of clinical research experience.
• At least 2 years of EDC data entry experience.
• At least 2 years of patient recruitment experience.
• Experience with oncology clinical research.
• Experience with EMR and EDC platforms.
• Strong attention to detail and data accuracy.
• Ability to multitask and manage scheduling.
• Effective communication with patients and clinical staff.

Responsibilities

• Pre-screen patients for oncology studies per protocol criteria.
• Conduct chart reviews to identify eligible participants.
• Enter data into EDC systems accurately and timely.
• Schedule appointments and send reminders.
• Verify data completeness and resolve queries.
• Review patient histories in EMR and document progress.
• Support patient recruitment by engaging potential participants.
• Collaborate with nurses and research team for study procedures.
• Maintain confidentiality and comply with guidelines.
• Work in a fast-paced setting with attention to detail and protocols.

Skills

Clinical research exp

EDC data entry

Patient recruitment

Oncology trials

EMR chart review

Data integrity

Scheduling coordination

Communication with patients

Job description

Actalent is seeking a part-time Clinical Research Coordinator (Oncology) based in New Brunswick, NJ. The role focuses on coordinating oncology studies, data management, scheduling, and regulatory adherence in a fast-paced clinical research environment.

You will work with clinical teams to pre-screen patients, verify eligibility, and maintain high-quality data in EMR and EDC systems while ensuring patient confidentiality and protocol compliance.