Job Description
Join our award-winning clinical research team at MediVance Research Institute, where innovation meets compassionate care. We seek a Clinical Research Nurse Coordinator to drive groundbreaking studies in oncology and immunotherapy. This role combines hands-on patient care with protocol management in a cutting-edge academic-medical partnership. Enjoy competitive compensation, comprehensive benefits, and opportunities for professional growth in one of America's premier healthcare hubs.
Responsibilities
- Oversee clinical trial protocols including patient recruitment, enrollment, and retention strategies
- Manage complex patient assessments and coordinate multidisciplinary care teams
- Maintain precise electronic medical records and regulatory documentation
- Administer investigational therapies and monitor adverse events per FDA guidelines
- Collaborate with biostatisticians on data integrity and protocol amendments
- Educate patients and families on trial procedures and informed consent
- Represent the institute at FDA audits and sponsor meetings
Qualifications
- BSN with minimum 3 years clinical research or oncology nursing experience
- ACRP or SOCRA certification strongly preferred
- Expertise in GCP/ICH guidelines and FDA regulatory requirements
- Proficiency with electronic health records (Epic, Medidata Rave)
- Certification in Basic Life Support (BLS) and Advanced Cardiac Life Support (ACLS)
- Exceptional communication skills for patient education and team collaboration
- Demonstrated ability to manage complex protocols and regulatory documentation