Clinical Research RN Supervisor

About the role

AdventHealth South Orlando is hiring a full-time day-shift Clinical Research RN Supervisor. The role plans, organizes and manages clinical research protocols, supervises the clinical research team and supports the operational manager. The position is based in Orlando, Florida.

Key responsibilities

• Deliver effective and compliant clinical research study coordination, including planning, organizing and managing activities related to clinical research protocols.
• Support the preceptorship of new team members, monitor their progress and communicate with the Operational Manager.
• Manage the clinical space used for protocols, overseeing set-up and turnover procedures per SOPs.
• Maintain clinical competencies such as physical assessment, phlebotomy and IV insertion, and apply Universal Precautions.
• Keep inventory levels adequate, order approved equipment and supplies, and maintain clinical supply areas.
• Develop and maintain Standard Operating Procedures (SOPs) and ensure teams follow them.
• Provide guidance, training and mentorship to study team members, and lead talent acquisition, team development and performance management.
• Act as a service line expert and resource for the research team, and manage safe, respectful patient care.
• Supervise daily team activity, including productivity, personnel and staffing schedules, and evaluate quality and safety of operations.
• Collaborate with the operations manager, study intake, research services and external partners on timely start-up and smooth transitions.

Required profile

• Registered Nurse (RN); Associate's degree in nursing required, Bachelor's preferred.
• 2+ years of clinical research experience; 4+ years with increasing people management responsibilities preferred.
• Ability to supervise clinical research teams, lead independently and communicate effectively in English; bilingual English/Spanish preferred.
• Knowledge of FDA, CDC and DHHS regulations governing clinical research, and of the regulatory process for investigational research.
• Licenses: RN and Basic Life Support (CPR) required; ACLS, CCRC, SOCRA certification preferred.

Required skills

• Proficiency with a clinical trials management system (CTMS).
• Microsoft Outlook, Word, Excel and Access.
• Ability to coordinate multiple clinical trials and solve problems quickly in a fast-paced environment.

What we offer

• Medical, dental, vision, life and disability insurance from day one.
• Paid time off and 4 weeks of 100% paid parental leave.
• 403(b) retirement plan and career development resources.
• Pay range of $68,806.40 to $120,723.20.