✨ About The Role
- This position involves coordinating investigational and research protocols, ensuring compliance with regulatory guidelines.
- The role requires attending meetings to gather information on clinical research projects and acting as a resource for staff and sponsors.
- Responsibilities include maintaining accurate data collection and reporting, as well as developing patient tracking systems.
- The candidate will assist in educating patients about research studies and obtaining informed consent.
- The position may involve developing and maintaining regulatory documents and assisting in budget management for research projects.
âš¡ Requirements
- The ideal candidate should have established oncology or research experience, demonstrating a solid understanding of clinical trials and protocols.
- Strong organizational skills are essential for coordinating various aspects of research projects, including subject recruitment and data collection.
- The candidate should possess excellent communication skills to effectively interact with patients, staff, and regulatory agencies.
- A background in nursing or a related healthcare field is preferred, with a commitment to patient advocacy and ethical research practices.
- The ability to work collaboratively with a diverse team of professionals in a fast-paced environment is crucial for success in this role.