Clinical Research Coordinator (Not a Remote)

Overview

Qualifications

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

Responsibilities

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.