What are the responsibilities and job description for the Clinical Research Coordinator position at Virginia Oncology Associates?
Overview :
Virginia Oncology Associates, the largest group of medical professionals in Hampton Roads and Northeast North Carolina devoted exclusively to cancer care and blood disorders, has an exciting opportunity for a Clinical Research Coordinator or a Clinical Research RN for our office in Norfolk and Hampton.
Please take this quick survey once you've submitted your resume to complete the application process : Clinical Research PI Link
Responsibilities :
Screening potential patients for protocol eligibility and presenting trial concepts and details to patients
Participating in the informed consent process and enrolling patients on protocol
75% of the job will be computer based and direct patient care is limited in a Clinical Research Coordinator role
Coordinating patient care in compliance with protocol requirements
Collaborating with the physician to review patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to drug study and thoroughly documenting all findings
Working directly with other research bases and / or sponsors
Overseeing the preparation of orders by physicians to assure that protocol compliance is maintained
Communicating with physicians regarding study requirements, need for dose modification and adverse event reporting
Qualifications :
Associates degree in a clinical or scientific related discipline required
Experience in clinical research preferred
Experience with computer data entry and database management
Excellent written and oral communication skills
Ability to read, analyze, and interpret technical procedures such as protocols, informed consent, and regulatory documents
Additional Qualifications for Nurse Candidates :
Graduate from an accredited program for nursing education (BSN preferred) preferred
Minimum of one (1) year nursing experience preferably in oncology
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