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Posted: 25-May-23
Location: Orlando, Florida
Salary: Open
Categories:
Internal Number: 23007729
Description
All the benefits and perks you need for you and your family:
- Benefits from Day One
- Paid Days Off from Day One
- Student Loan Repayment Program
- Career Development
- Whole Person Wellbeing Resources
- Mental Health Resources and Support
- Pet Insurance*
- Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense)
Our promise to you:
Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better.
Schedule: Full-Time
Shift: Day
The role you’ll contribute:
The Supervisor, Clinical Research serves the AdventHealth Research Institute (AHRI) providing oversight of the conduct of industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, Food and Drug Administration (FDA) regulations and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) guidelines. The Supervisor functions as a clinical study coordinator and serves to assist in the mentoring and developing of clinical study coordinators and research staff in the conduct of clinical research within the AdventHealth research enterprise at the institute level. Works closely with AHRI Core Managers to schedule clinical operations to facilitate the initiation and completion of clinical research studies. Assists the manager with day to day supervision and annual evaluation of clinical research staff at the department level. Actively participates in outstanding customer service and accepts responsibility for maintaining relationships that are equally respectful to all.
The value you’ll bring to the team:
- Delivers safe care and demonstrates regard for the dignity and respect of all participants. Maintains adequate skills in clinical competencies including but not limited to physical assessment, phlebotomy and IV insertion. Practices the principles of Universal Precautions. Understands and abides by HIPAA regulations.
- Maintains a clean, prepared clinical space. May perform set-up and turnover procedures in all clinical areas, per SOP’s, in a timely manner.
- Participates in internal and/or external training programs to maintain licensure.
- Performs a variety of supervisory duties including, but not limited to, selection, oversight, development, and performance management of research staff including positive discipline and annual evaluations. Supervises day to day activity of the research team within their assigned area, including personnel and staffing schedules as affected by research protocols at any given time.
- Assists Clinical Operations Manager with maintaining adequate inventory levels, ordering of approved equipment and supplies, maintenance of medical tools (biopsy needles, etc.) and clinical supply areas
- Provides effective and compliant clinical research study coordination, including planning, organizing, and managing all activities related to clinical research operations and execution of timelines
- Collaborates with AdventHealth Research Institute (AHRI) Core Managers/Supervisors within various inpatients and outpatient clinical settings to develop and implement processes that ensure workflow and scheduling are optimized for day to day operations.
- Interfaces with AHRI Cores as study coordinator and supervisor to ensure initiation and completion of industry-sponsored and investigator-initiated clinical trials
- Under the direction of the Clinical Research Operations Manager, develops and maintains Standard Operating Procedures (SOPs) for the teams they supervise, and ensures clinical research operations teams follow AHRI processes and procedures.
- Develops approaches to monitor and evaluate the quality and safety of clinical operations within their assigned department.
The expertise and experiences you’ll need to succeed:
EDUCATION AND EXPERIENCE REQUIRED:
- Bachelor’s degree in Nursing and two (2) years of clinical research experience or
- Associates degree in Nursing and four (4) years of clinical research experience
LICENSURE, CERTIFICATION OR REGISTRATION REQUIRED:
- Certified Clinical Research Coordinator (CCRC) (per the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA))
- Current, active State of Florida Nursing License
- BLS
EDUCATION AND EXPERIENCE PREFERRED:
-
- Master’s degree in Nursing or related field
- 5 years of clinical research experience with increasing people management responsibilities
