Clinical Research Coordinator, RN

Responsibilities

• Responsible for study coordination and data management with a focus on managing subject recruitment and enrollment
• Maintain site compliance for all clinical trial activities and regulations
• Complete all relevant Profound Research required training in a timely manner
• Educates and directs protocol compliance with physicians and staff
• Ensure good documentation practices are applied by all team members
• Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors
• Acts as a patient advocate
• Collaborates with scheduling staff and the physician to assure appointments are scheduled correctly and treatment orders are written and delivered

• Must be a Registered Nurse (RN) with a current and valid license
• Associate’s or Bachelor’s degree in Nursing (ASN or BSN) required
• 2 or more years Nursing experience in ICU, ER, oncology or clinical trial experience, preferred
• Ability to Start IVs and Administer IV medications
• Ability to draw blood
• Understanding of all aspects of biomedical research protocols, ensuring applicable regulations, and guidelines
• Skill in using computer programs and applications including Microsoft Office