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

Clinical Research Coordinator- Phase II-III - Full-Time - Wolf River

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.

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

Associate's degree or equivalent from a two-year college or technical school

Minimum of 12 years of related clinical research experience, or successful completion of 1 year as an Associate Clinical Research Coordinator I

Preferred: Registered Nurse (RN) certification

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

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.

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.