Job Description

Minimum Qualifications
One of the following
Associate degree with minimum 1 of the most recent 3 years’ clinical oncology research experience
Minimum 3 of most recent 5 years’ clinical oncology research experience
Must have
Problem solving, analytical, resource management, and creative thinking skills
Ability to plan and schedule tasks and projects and complete them in a timely manner
Ability to delegate duties while maintaining responsibility for completion of tasks
Ability to maintain confidentiality of sensitive information
Licensure, Registration, Certification
BLS
One of the following
Certified Clinical Research Coordinator (CCRC) through the Association of Clinical Research Professionals (ACRP)
Certified Clinical Research Professional (CCRP) through the Society of Clinical Research Associates (SOCRA) certification
If not currently certified in CCRC or CCRP, certification must be obtained within 12 months of qualification for exam
Desired Qualifications
BSN or higher degree
Understanding of Good Clinical Practice (GCPs) and all regulatory requirements of the FDA
Working knowledge of word processing and PC based programs
Licensure, Registration, Certification
CCCR/CCRP Certification
ACLS
The Coordinator Clinical Research (CCR) is responsible for coordinating the daily clinical activities of patients enrolled on clinical trials. Duties will include screening potential study patient records, enrolling patients on protocol and ensuring all protocol specific tests/procedures are scheduled and complete. Ensures compliance with Institutional, IRB, FDA, and sponsor guidelines/regulations and standard operating procedure requirements. The CCR is also responsible for demonstrating professional demeanor and maintaining confidentiality in all interactions with both internal and external contacts.

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