Clinical Research Supervisor

Clinical Research Supervisor

The Clinical Research Supervisor is responsible for overseeing the conduct of both industry-sponsored and investigator-initiated clinical trials in alignment with trial protocols, FDA regulations, and ICH/GCP guidelines. This role involves acting as a clinical study coordinator while also mentoring and developing clinical study coordinators and research staff within the research enterprise at the institute level.

Responsibilities:

• Provide oversight of clinical trials to ensure adherence to trial protocols, FDA regulations, and ICH/GCP guidelines.
• Function as a clinical study coordinator and assist in mentoring clinical study coordinators and research staff.
• Work closely with Core Managers to schedule clinical operations and facilitate the initiation and completion of clinical research studies.
• Assist the manager with daily supervision and annual evaluations of clinical research staff.
• Maintain clinical competencies in physical assessment, phlebotomy, and IV insertion, while practicing Universal Precautions and adhering to HIPAA regulations.
• Ensure cleanliness and preparedness of clinical spaces, including set-up and turnover procedures according to SOPs.
• Participate in training programs to maintain licensure.
• Perform supervisory duties such as selection, oversight, development, and performance management of research staff.
• Supervise daily activities of the research team, including staffing schedules affected by research protocols.
• Assist Clinical Operations Manager in maintaining inventory levels, ordering equipment and supplies, and maintaining clinical supply areas.
• Provide effective clinical research study coordination, including planning, organizing, and managing all related activities.
• Collaborate with AHRI Core Managers to optimize workflow and scheduling for daily operations.
• Interface with AHRI Cores to ensure initiation and completion of clinical trials.
• Develop and maintain SOPs under the direction of the Clinical Research Operations Manager.
• Monitor and evaluate the quality and safety of clinical operations within the department.

Essential Skills:

• Bachelor's degree in Nursing
• Two years of clinical research experience or experience as a clinical research nurse
• Certified Clinical Research Coordinator (CCRC)
• Current, active State of Florida Nursing License
• Basic Life Support (BLS) certification

Additional Skills & Qualifications:

• Master's degree in Nursing is preferred
• Five years of clinical research experience with increasing people management responsibilities is preferred
• Advanced Cardiovascular Life Support (ACLS) certification is preferred
• Other applicable certifications such as medical assistant, medical technician, or phlebotomy

Work Environment:

The position is based on campus and involves collaboration with various clinical settings to implement processes that optimize workflow and scheduling for day-to-day operations. The work environment includes maintaining a clean and prepared clinical space, and adherence to all safety and regulatory guidelines.

Job Type & Location:

This is a Permanent position based out of Orlando, FL.

Pay and Benefits:

The pay range for this position is $90000.00 - $115000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Paid Time Off from Day One 403-B Retirement Plan 4 Weeks 100% Paid Parental Leave Career Development Whole Person Well-being Resources Mental Health Resources and Support Pet Benefits

Workplace Type:

This is a fully onsite position in Orlando, FL.

Application Deadline:

This position is anticipated to close on Aug 31, 2026.