Oncology Study Coordinator: Lead Multisite Clinical Trials

ECLARO; Chapel Hill (NC); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

401(k) Retirement Savings Plan

Commuter Check Pretax Benefits

Medical, Dental & Vision Insurance

Job summary

ECLARO is seeking a Study Coordinator for our client in Chapel Hill, NC to independently coordinate and manage multiple oncology clinical trials throughout the study lifecycle. You will work with Principal Investigators, sponsors, and clinical teams to ensure trials adhere to protocol, GCP, and regulatory requirements.

Responsibilities include site visits, enrollment, data collection, biospecimen handling, and audits.

Qualifications

• Experience as a study coordinator or in oncology clinical trials.
• Familiar with Phase I-III clinical research including investigational drugs/devices.
• Experience coordinating complex studies independently.

Responsibilities

• Independently manage multiple oncology clinical trials from startup through closeout.
• Maintain understanding of assigned study protocols and sponsor requirements.
• Coordinate activation, implementation, monitoring, and closure activities.
• Participate in site initiation visits, startup meetings, monitoring visits, and closeout visits.
• Maintain study documentation and regulatory records.
• Identify, screen, recruit, and enroll eligible research participants.
• Conduct informed consent discussions and document patient participation.
• Coordinate protocol-required study visits and data collection.
• Enter study data into electronic data capture systems and case report forms.
• Resolve data queries within established timelines.
• Coordinate collection, processing, storage, and shipment of research specimens.
• Ensure compliance with GCP, FDA and Federal Regulations.
• Track time and effort reporting; support administrative functions.
• Collaborate with investigators, sponsors, and clinic staff; train new members.

Skills

Clinical Research Expertise

Operational Skills

Communication & Collaboration

Job description

ECLARO is seeking a Study Coordinator for our client in Chapel Hill, NC to independently coordinate and manage multiple oncology clinical trials throughout the study lifecycle. You will work with Principal Investigators, sponsors, and clinical teams to ensure trials adhere to protocol, GCP, and regulatory requirements.

Responsibilities include site visits, enrollment, data collection, biospecimen handling, and audits.