This position is responsible for coordinating and implementing assigned protocols while collecting and recording medical data and history
Job Summary
This position is responsible for coordinating and implementing assigned protocols while collecting and recording medical data and history.
The role involves assisting in the recruitment and screening of volunteers, obtaining informed consent, and ensuring compliance with FDA and institutional regulations.
Candidates will serve as a liaison between patients, families, physicians, and other departments to ensure safe and ethical trial treatment options.
Matching Summary
This position is responsible for coordinating and implementing assigned protocols while collecting and recording medical data and history.
Skills & Requirements
Must-have
Knowledge of clinical research methodologies
Experience with FDA and institutional regulations
Ability to maintain patient confidentiality
Excellent organizational and task management skills
Familiarity with medical and clinical terminology
Nice-to-have
Established Oncology experience
Friendly work environment
Career growth opportunities
Strong human relations skills
Passionate commitment to patient care
Key Requirements
Bachelor's degree in a healthcare field
Two to four years of clinical research experience
Clinical Research Coordinator Certification (CRCC) preferred