✨ About The Role
- This position involves coordinating investigational and research protocols, including project preparation, subject recruitment, and data collection.
- The role requires ensuring that clinical research staff conduct projects appropriately and adhere to clinical trial schedules.
- The candidate will develop and maintain regulatory and legal documents in compliance with guidelines from various regulatory agencies.
- Accurate data collection and reporting according to protocol requirements are critical responsibilities of this position.
- The role includes educating patients about research studies and assisting in obtaining informed consent from participants.
- The candidate will also assist in the development and maintenance of budgets and contract agreements related to research projects.
âš¡ Requirements
- A successful candidate will possess a thorough knowledge of nursing and healthcare, typically demonstrated through a Bachelor's Degree in Nursing.
- The role requires a current Registered Nurse (R.N.) license and at least two years of clinical research experience or relevant experience in the clinical area of the research study.
- Excellent organizational and task management skills are essential, along with the ability to maintain confidentiality of patient and study information.
- Strong human relations, organizational, and communication skills are necessary to effectively collaborate with various clinical and administrative positions.
- The ideal candidate should have the ability to conduct computer-based literature searches and stay updated on Federal and State regulations governing practice.