West Cancer Center is looking to hire a Clinical Research Coordinator to manage oncology patients participating in pharmaceutical-sponsored clinical trials, ensuring compliance with study protocols and regulatory standards.
Requirements
- Minimum of 1–2 years of related clinical research experience, or successful completion of 1 year as an Associate Clinical Research Coordinator I
- Strong knowledge of clinical research regulations, data management, and patient safety
- Ability to analyze complex data and interpret technical documents
- Competence in performing necessary calculations (BSA, ANC, drug dosing)
- Proficiency in computer applications, including word processing and email
- 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
- 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
Other
- Associate’s degree or equivalent from a two-year college or technical school
- Strong organizational, follow-up, and problem-solving skills
- Excellent verbal and written communication abilities
- Ability to manage multiple priorities in a fast-paced environment
- Ability to collaborate effectively within multidisciplinary teams
