Research Coordinator II
Core
Lead Research Coordinator managing clinical trial operations, patient recruitment, eligibility screening, and protocol compliance for oncology studies.
Role type
Senior IC clinical research coordinator
Builds
Clinical trial operations and patient care pathways
Domain
Healthcare / Oncology Clinical Trials
Required skills
Protocol compliance monitoring, patient eligibility screening, informed consent management, adverse event reporting, drug dose calculation, specimen handling, data entry, regulatory audit preparation
Preferred skills
Prior experience as a protocol coordinator, knowledge of FDA/NCI regulations, experience with investigational drug logistics
Technologies
iStar, CAFE database, hospital databases
Responsibilities
Review new protocols for feasibility and budget impact; screen patients for eligibility and obtain informed consent; schedule study tests and follow-up appointments; calculate drug doses and manage toxicity assessments; coordinate blood draws and specimen transport; report Serious Adverse Events; interact with physicians, patients, and hospital staff; assist with data management and study result generation.