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ClinLab Solutions Group · Freehold, New Jersey
Clinical Research Coordinator, Oncology
A leading community oncology practice is seeking a Clinical Research Coordinator to manage oncology clinical trials. This is a full time, onsite role where you will own assigned trials from start to finish and help bring cutting edge cancer treatments to patients close to home.
Serve as the main point of contact for assigned oncology interventional trials, ensuring protocol requirements are understood and followed.
Screen, recruit, and enroll patients using EMR, EDC, and CTMS, and maintain enrollment logs for each study.
Schedule and track patient visits, infusions, imaging, EKGs, and labs required by the protocol.
Enter study data into EDC and EMR within 24 hours of collection and resolve data queries within 5 days.
Monitor and report adverse events, serious adverse events, and protocol deviations within 24 hours to the investigator and study leadership.
Oversee study kits, investigational drug accountability, and drug destruction records.
Process, ship, and store biological specimens according to sponsor protocols, IATA regulations, and biohazard precautions.
Assist with collecting and maintaining regulatory documents and support internal and external audits.
Attend sponsor visits including SIVs, IMVs, and COVs, and lead weekly and monthly trial meetings.
Collaborate with physicians, nurses, pharmacy, and clinic staff to keep workflows aligned with protocol requirements.
Track and submit patient reimbursement for clinical trial participation.
ACRP (CCRC or CCRA) or SoCRA (CCRP) certification preferred; a high school diploma with 4 years of oncology trial experience will also be considered.
Strong communication, organization, and time management skills with the ability to thrive in a fast paced clinic environment.
Details
| Company | ClinLab Solutions Group |
| Location | Freehold, New Jersey |
| Type | FULL TIME |
| Niche | Full-time |