Oncology Trials Coordinator – Onsite

Actalent; Raleigh (NC); On-site; USD 45,000 - 48,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

Time Off/Leave (PTO)

Job summary

Actalent is seeking an Oncology Clinical Research Coordinator for a fully onsite role in Chapel Hill/Raleigh, NC. You will independently manage multiple oncology trials from startup through closeout, serving as the primary contact among patients, physicians, sponsors, and staff.

The role demands coordination of all trial phases, patient recruitment, data entry, and regulatory oversight. Onsite 5 days a week with relocation to the Chapel Hill area required; compensation includes standard benefits

Qualifications

• 1+ year of CRC or Study Coordinator experience.
• Experience in recruitment, screening, consent, enrollment, and scheduling.
• Proficiency with Electronic Data Capture systems (e.g., Medidata Rave, Oracle, Inform).
• Regulatory experience including IRB submissions/maintenance and study documentation.

Responsibilities

• Coordinate all phases of clinical trials from activation to closeout.
• Recruit, screen, consent, and enroll study participants.
• Schedule protocol-required patient visits and follow-ups.
• Educate patients and serve as a study resource throughout participation.
• Enter study data and maintain source documentation.
• Manage regulatory records and ensure compliance with study requirements.
• Support sponsor monitoring visits, audits, and inspections.
• Coordinate collection, processing, and shipment of research specimens.
• Report adverse events and protocol deviations.
• Collaborate with investigators, sponsors, nurses, and staff on startup and closeout activities.

Skills

CRC experience

Recruitment & enrollment

Electronic Data Capture

Regulatory compliance

Study data management

Monitoring & audits

GCP/FDA knowledge

Oncology/CNS experience

Education

Bachelor’s degree in science/healthcare

Tools

Epic/EMR

Job description

Actalent is seeking an Oncology Clinical Research Coordinator for a fully onsite role in Chapel Hill/Raleigh, NC. You will independently manage multiple oncology trials from startup through closeout, serving as the primary contact among patients, physicians, sponsors, and staff.

The role demands coordination of all trial phases, patient recruitment, data entry, and regulatory oversight. Onsite 5 days a week with relocation to the Chapel Hill area required; compensation includes standard benefits