Clinical Research Coordinator 2
Core
Coordinates daily activities of moderately complex clinical oncology trials, managing patient recruitment, data collection, and regulatory compliance.
Role type
Mid-level clinical research coordinator (oncology)
Builds
Clinical trial data and patient records for investigator-initiated and industry-sponsored studies
Domain
Healthcare + Clinical Research
Required skills
Clinical trial coordination, patient recruitment, informed consent, adverse event reporting, case report form completion, specimen handling, IRB submission, protocol adherence, data confidentiality, SOP implementation, record maintenance
Preferred skills
Multi-study coordination, clinical research experience, complex protocol interpretation, problem solving, time management, Microsoft Office proficiency, regulatory compliance knowledge
Technologies
Microsoft Office (Outlook, Word, Excel), clinical research databases, electronic systems
Responsibilities
Recruit and interview potential study patients; collect, process, and store biological specimens; coordinate study procedures and patient schedules; prepare and submit IRB applications; ensure compliance with federal regulations and institutional policies; maintain accurate research records including CRFs and drug logs; educate patients on study procedures and risks.
Seniority
Mid-level, limited to moderate supervision