Experienced Clinical Research Associate - Hematology/Oncology
Core
Conduct qualification, initiation, monitoring, and closeout visits at research sites to ensure compliance with protocols and regulatory requirements for hematology/oncology clinical trials.
Role type
Clinical Research Associate (Hematology/Oncology)
Builds
Clinical trial data integrity and regulatory compliance for biopharma/medical device projects
Domain
Clinical Research / Hematology & Oncology
Deliverable
physical/clinical work
Required skills
Clinical trial monitoring, protocol deviation management, source data verification, adverse event reporting, site qualification, regulatory document review, patient recruitment assessment
Preferred skills
Hematology/oncology therapeutic area expertise, risk-based monitoring approach
Technologies
Clinical Trial Management System (CTMS), Microsoft Office
Responsibilities
Conduct on-site and virtual monitoring activities; verify investigator qualifications and resources; review medical records and source documentation; assess patient recruitment and retention; complete monitoring reports and follow-up letters.
Seniority
Entry-level to Mid-level (minimum 1 year experience)
