Clinical Research Coordinator - Full-Time - Wolf River

West Cancer Center•Germantown, TN

10d

About The Position

At West Cancer Center, we are dedicated to providing compassionate, patient-centered care while advancing groundbreaking research. Our team fosters collaboration, innovation, and professional growth, ensuring that every role contributes to making a difference in patients’ lives. Join us in our mission to provide comprehensive support to those navigating the challenges of cancer treatment. The Clinical Research Coordinator plays a vital role in managing oncology patients participating in pharmaceutical-sponsored clinical trials. This position is responsible for patient screening, enrollment, education, and ongoing monitoring to ensure compliance with study protocols and regulatory standards. The ideal candidate will have prior experience managing clinical trials and a strong understanding of Good Clinical Practice (GCP) and FDA regulations.

Requirements

Associate’s degree or equivalent from a two-year college or technical school
Minimum of 1–2 years of related clinical research experience, or successful completion of 1 year as an Associate Clinical Research Coordinator I
Strong organizational, follow-up, and problem-solving skills
Excellent verbal and written communication abilities
Ability to manage multiple priorities in a fast-paced environment
Proficiency in computer applications, including word processing and email
Ability to collaborate effectively within multidisciplinary teams
Strong knowledge of clinical research regulations, data management, and patient safety
Comfort working near potentially hazardous materials
Ability to analyze complex data and interpret technical documents
Competence in performing necessary calculations (BSA, ANC, drug dosing)
Ability to travel as required

Nice To Haves

Registered Nurse (RN) certification

Responsibilities

Recruit and screen potential clinical trial subjects
Conduct detailed review of patient medical history and current findings for eligibility
Educate nursing staff on proper administration and side effects of study therapies
Educate patients on study protocols, medication adherence, and symptom management
Act as a liaison between the Research Team and non-research clinical staff
Maintain patient safety, rights, and informed consent throughout the study
Ensure regulatory compliance and maintain current knowledge of the Code of Federal Regulations
Monitor study progress and patient outcomes
Interface with multiple departments, including Physicians, Nurses, Radiology, Medical Records, Laboratory, Insurance, and Pharmacy
Document all relevant patient and study information accurately
Maintain a professional demeanor and uphold confidentiality at all times
Perform other duties as assigned