Clinical Research Coordinator- Phase I - Full-Time - Wolf River
On-site · Germantown, Tennessee, United States
Job Summary
Clinical Research Coordinator at West Cancer Center focused on managing oncology patients in pharmaceutical-sponsored phase I trials. Responsibilities include recruiting and screening potential trial subjects, reviewing medical histories for eligibility, educating nursing staff and patients on study protocols, medication adherence, and symptom management, acting as a liaison between the research team and clinical staff, ensuring patient safety, rights, and informed consent, maintaining regulatory compliance with CFR and GCP, monitoring study progress and patient outcomes, interfacing with physicians, nurses, radiology, medical records, laboratory, insurance, and pharmacy, documenting all study-related information accurately, and performing other duties as assigned. Requires an Associate’s degree or equivalent with 1–2 years of clinical research experience (RN certification preferred), strong organizational and communication skills, ability to manage multiple priorities, proficiency with common software, collaboration across multidisciplinary teams, knowledge of regulatory requirements, comfort with hazardous materials, data interpretation, calculations (BSA, ANC, dosing), and willingness to travel. No nights, weekends, or holidays; comprehensive benefits; remote-work not indicated. The role is located at the West Cancer Center in Germantown, TN.
Required Qualifications
- 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
- 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
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