✨ About The Role
- This position involves coordinating investigational and research protocols within the oncology service line.
- The role requires promoting research study initiation and acting as a liaison between various stakeholders, including sponsors and regulatory agencies.
- Responsibilities include ensuring clinical research staff adhere to trial schedules and assisting in obtaining informed consent from participants.
- The candidate will develop and maintain regulatory documents and assist in annual reporting to federal agencies.
- The job entails educating patients about research studies and performing medical record reviews to support patient recruitment and treatment.
âš¡ Requirements
- A successful candidate will have experience in clinical research coordination and a strong understanding of oncology protocols.
- The ideal individual should possess excellent communication skills to effectively interact with patients, staff, and regulatory agencies.
- A background in nursing is essential, with a focus on patient advocacy and ethical treatment practices.
- The candidate should be detail-oriented, capable of managing multiple research projects simultaneously while ensuring compliance with regulations.
- Experience in data collection and reporting is crucial for maintaining the integrity of clinical trials.