Clinical Research Coordinator; Oncology

Benefits

Qualifications

• •3+ years of experience as a Clinical Research Coordinator
• •At least 1 year of oncology clinical trial experience
• •Experience serving as primary CRC on multiple drug and/or device trials
• •Strong patient‑facing experience in a healthcare or research setting
• •Bachelor’s degree in a science or related field (or equivalent experience)
• •Experience with EDC systems and CTMS platforms
• •Ability and willingness to work fully onsite
• •Willingness to obtain one of the following within 12 months:
• •CCRP (SOCRA)
• •CCRC (ACRP or SCRA)
• •Certified Phlebotomy Technician (ANCC)
• •8 more items(s)

Responsibilities

• •te role supporting patient‑facing research activities from study start‑up through close‑out
• •This is a net‑new, urgent opening with a strong likelihood of extension and potential conversion to a full‑time role
• •Coordinate and execute oncology clinical trials under the direction of Principal Investigators
• •Recruit, screen, consent, and enroll research participants
• •Coordinate and conduct protocol‑required visits, procedures, labs, and assessments
• •Collect, enter, and report study data per protocol and sponsor requirements
• •Process, handle, and ship biological specimens in accordance with federal regulations
• •Support study drug accountability and coordinate medication administration
• •Identify and report adverse events, SAEs, protocol deviations, and violations
• •Participate in sponsor monitoring visits, audits, and inspections
• •Serve as a liaison between patients, investigators, sponsors, IRBs, and clinical teams
• •Maintain inspection and audit readiness across studies
• •9 more items(s)