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  3. Clinical Research Coordinator- Phase II-III - Full-Time - Wolf River - Registered Nurse (RN) Preferred
WC

Clinical Research Coordinator- Phase II-III - Full-Time - Wolf River - Registered Nurse (RN) Preferred

West Cancer Center·Germantown, Tennessee

Full Time·On Site·0-2 yrs·
Posted 3 days ago
Practice for this role

About the role

The Clinical Research Coordinator manages oncology patients in pharmaceutical-sponsored clinical trials, focusing on screening, enrollment, and monitoring. They act as a liaison between the research team and clinical staff to ensure protocol compliance and patient safety.

Job Title

Clinical Research Coordinator- Phase II-III About Us 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. Position Overview 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. Key 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

Qualifications

Education & Experience 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 Preferred: Registered Nurse (RN) certification Skills & Abilities 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 Why West Cancer Center is a Great Place to Work Meaningful Impact: Play a direct role in supporting patients through one of the most challenging times of their lives. Collaborative Culture: Work alongside a multidisciplinary team of dedicated professionals committed to improving cancer care. Professional Development: Benefit from ongoing training, educational resources, and growth opportunities. Mission-Driven Environment: Be part of an organization guided by compassion, integrity, and innovation. No nights, weekends, or holidays. Comprehensive benefits package. Join Us If you are a detail-oriented clinical research professional looking to make a difference in oncology care, apply today to become a Clinical Research Coordinator at West Cancer Center.

Requirements

Candidates need an associate's degree and 1-2 years of clinical research experience, with an RN certification preferred. Proficiency in GCP, FDA regulations, and clinical data calculations is required.

  • associate degree
  • professional certificate
  • Regulatory Compliance
  • Patient Education
  • Patient Safety
  • Medical History Review
  • Data Management
  • Multidisciplinary Collaboration
  • Informed Consent
  • Patient Screening
  • FDA Regulations
  • Clinical Trial Management
  • Good Clinical Practice (GCP)
  • Drug Dosing Calculations

Benefits

  • Comprehensive Benefits Package

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
0-2 yrs
Location
Germantown, Tennessee
Posted
Jul 24, 2026
Application
Employer website
WC

Hiring organization

West Cancer Center

West Cancer Center & Research Institute is proud to be the region’s comprehensive leader in adult cancer care and research. After delivering 40 years of clinical excellence, our focus still remains the same. We strive to continuously fight for the best outcomes for our patients...

IndustryHospitals and Health Care
TypePartnership
Size501-1,000 employees
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Market context

Tennessee nursing roles need flexible RNs

In Tennessee, nursing roles often stay active because hospitals, clinics, and long-term care settings need licensed RNs who can cover full-time schedules and rotating shifts. These positions can be competitive when they include weekend, holiday, and call coverage, since employers usually look for candidates who can balance clinical skill with schedule flexibility. On this platform, the job requirements and benefits are AI-summarized from the original posting, helping you review key details faster before applying.

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