Clinical Research Coordinator 2 - Hematology/Oncology
Core
Manages all aspects of conducting moderately complex clinical trials in hematology/oncology, including patient recruitment, data collection, and regulatory compliance.
Role type
Clinical Research Coordinator 2 (moderately complex studies)
Builds
Clinical trial operations and patient data integrity
Domain
Healthcare / Clinical Research / Hematology & Oncology
Required skills
Clinical trial management, patient recruitment, informed consent, adverse event reporting, case report form completion, specimen handling, protocol adherence, IRB submission, data confidentiality, SOP implementation, audit participation
Preferred skills
Multi-study coordination, investigator-initiated trial experience, industry-sponsored trial experience, multi-site trial coordination
Technologies
Electronic Health Records (EHR), Case Report Forms (CRF), Laboratory Information Systems (LIS)
Responsibilities
Recruits and interviews potential study patients; Collects, processes, and stores specimens; Coordinates study conduct from startup to closeout; Educates patients on procedures and risks; Performs assessments and monitors adverse events; Maintains accurate research records and ensures regulatory compliance; Prepares IRB submissions; Assists in training new coordinators.
Seniority
Mid-level, independent contributor