Clinical Research Coordinator (Not a Remote)

Infirmary Health; Mobile (AL); Remote; USD 55,000 - 75,000; Full time

Job summary

A leading healthcare organization is seeking a Coordinator Clinical Research to manage clinical trial activities. The ideal candidate will have a strong background in oncology research, relevant certifications, and excellent problem-solving skills. This role involves coordinating patient enrollment, ensuring compliance with regulatory standards, and maintaining confidentiality in all interactions.

Qualifications

• Minimum 1 year of recent clinical oncology research experience or 3 years in the past 5 years.
• BLS certification and one of CCRC or CCRP required.
• Certification must be obtained within 12 months if not currently certified.

Responsibilities

• Coordinate daily clinical activities of patients in clinical trials.
• Screen potential study patients and enroll them on protocols.
• Ensure compliance with institutional, IRB, FDA, and sponsor guidelines.

Skills

Problem-solving

Analytical

Resource management

Creative thinking

Education

Associate degree

Bachelor of Science in Nursing (BSN)

Tools

Word processing

PC-based programs

Job description

Overview

Qualifications

Minimum Qualifications:

1. Associate degree with a minimum of 1 year of recent clinical oncology research experience, or
2. At least 3 years of recent clinical oncology research experience within the past 5 years.

Must have:

1. Problem-solving, analytical, resource management, and creative thinking skills.
2. Ability to plan, schedule, and complete tasks and projects in a timely manner.
3. Ability to delegate duties while maintaining responsibility for their completion.
4. Ability to maintain confidentiality of sensitive information.

Licensure, Registration, Certification:

• BLS certification.
• One of the following certifications:
• Certified Clinical Research Coordinator (CCRC) through ACRP, or
• Certified Clinical Research Professional (CCRP) through SOCRA.

If not currently certified, certification must be obtained within 12 months of qualification for the exam.

Desired Qualifications:

• Bachelor of Science in Nursing (BSN) or higher degree.
• Understanding of Good Clinical Practice (GCPs) and all FDA regulatory requirements.
• Working knowledge of word processing and PC-based programs.
• Additional certifications: CCRP/CCRP, ACLS.

Responsibilities

The Coordinator Clinical Research (CCR) is responsible for coordinating the daily clinical activities of patients enrolled in clinical trials. Responsibilities include screening potential study patient records, enrolling patients on protocols, scheduling and ensuring completion of all protocol-specific tests and procedures, and ensuring compliance with institutional, IRB, FDA, sponsor guidelines, and SOPs. The CCR must demonstrate professionalism and maintain confidentiality in all interactions with internal and external contacts.