Onsite Oncology Trial Coordinator — Lead Multi-Study Roles

Actalent; Atlanta (GA); On-site; USD 45,000 - 48,000; Full time

Benefits offered by this job

Medical benefits

401(k) retirement plan

Disability coverage

Job summary

Actalent is seeking an Oncology Clinical Research Coordinator for a fully onsite role in Chapel Hill, NC, with relocation required. You will independently manage multiple oncology trials, coordinating patient enrollment, visits, data entry, and regulatory compliance, while serving as the primary contact among patients, physicians, sponsors, and clinical teams.

The role requires at least 1 year CRC experience, proficiency with EDC systems, and familiarity with GCP/FDA regulations.

Qualifications

• At least 1 year CRC/Study Coordinator experience.
• Experience in patient recruitment, screening, informed 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.
• Experience managing study data, source documentation, and case report forms (CRFs).
• Experience with monitoring visits, audits, and query resolution.
• Knowledge of GCP, FDA regulations, and clinical research compliance.
• Oncology and/or Cardiovascular/CNS experience.

Responsibilities

• Coordinate all phases of clinical trials from startup through closeout.
• Recruit, screen, consent, and enroll study participants.
• Schedule and manage protocol-required patient visits and follow-up appointments.
• Educate patients and serve as a study resource throughout participation.
• Enter study data into systems and maintain accurate source documentation.
• Manage regulatory records and ensure ongoing compliance with study requirements.
• Support sponsor monitoring visits, audits, and study inspections.
• Coordinate collection, processing, tracking, and shipment of research specimens.
• Report adverse events (AE/SAE), protocol deviations, and other study-related issues.
• Collaborate with investigators, sponsors, nurses, laboratory personnel, and research staff on startup/closeout and process improvements.

Skills

CRC experience

Patient recruitment

EDC systems

Regulatory experience

GCP/FDA knowledge

Oncology experience

Education

Bachelor's degree

Tools

Medidata Rave

Oracle

Inform

Job description

Actalent is seeking an Oncology Clinical Research Coordinator for a fully onsite role in Chapel Hill, NC, with relocation required. You will independently manage multiple oncology trials, coordinating patient enrollment, visits, data entry, and regulatory compliance, while serving as the primary contact among patients, physicians, sponsors, and clinical teams.

The role requires at least 1 year CRC experience, proficiency with EDC systems, and familiarity with GCP/FDA regulations.