Clinical Research Supervisor Adult Oncology

AdventHealth Central Florida; Orlando (FL); On-site; USD 80,000 - 110,000; Full time

Job summary

A leading health care provider seeks a Clinical Research Supervisor for adult oncology in Orlando. This role is critical for overseeing clinical trials and managing the research staff. Ideal candidates will have relevant educational qualifications and significant experience in clinical leadership. Benefits include comprehensive health resources, paid time off, and educational opportunities.

Benefits

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

Nursing Clinical Ladder Program

Relocation Bonus

Qualifications

• Minimum 2 years of experience in clinical research (Bachelor's level).
• Preferred 5 years clinical research with people management.
• Basic Life Support (BLS) and Advanced Cardiovascular Life Support (ACLS) certifications.

Responsibilities

• Oversee clinical trials in accordance with protocols and regulations.
• Manage a team of clinical research coordinators and staff.
• Participate in the development of SOPs and maintain operational compliance.

Skills

Bilingual (English/Spanish)

People Management

Clinical Research Oversight

Customer Service

Education

Bachelor’s Degree in Healthcare Administration, Research, or related field

Associate's Degree in Healthcare Administration, Research, or related field

Master’s degree in Healthcare Administration, Research, or related field

Certified Clinical Research Coordinator (CCRC)

Job description

Clinical Research Supervisor Adult Oncology

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Clinical Research Supervisor Adult Oncology

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The expertise and experiences you’ll need to succeed\:

• Minimum qualifications\:
• Bachelor’s Degree in Healthcare Administration, Research, or related field and 2 years of experience in clinical research or
• Associates degree in Healthcare Administration, Research, or related field and 4 years of experience in clinical research or related field
• Basic Life Support (BLS) Certification
• Preferred qualifications:
• Bilingual (English/Spanish)
• Master’s degree in Healthcare Administration, Research, or related field
• 5 years of clinical research experience with increasing people management responsibilities
• Certified Clinical Research Coordinator (CCRC) (per the Association of Clinical Research
• Professionals (ACRP) or Society of Clinical Research Associates (SOCRA)
• Advanced Cardiovascular Life Support (ACLS)
• Other certification as applicable to degree or program (i.e. medical assistant, medical technician, phlebotomy)
• If licensed, (such as LPN), maintain current active State of Florida license
  
  

Clinical Research Supervisor Non-RN- AdventHealth Orlando

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)
• Nursing Clinical Ladder Program*
• Sign-on Bonus*
• Relocation Bonus*
• Team Based Nursing Model*
  
  

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\: M-F (8a – 4\:30p) may need flexibility based on physicians/surgeons schedules. No On call or weekends.

Travel: about 25% -30% of the time

Location\: 601 EAST ROLLINS STREET, Orlando, 32803

The community you’ll be caring for\: AdventHealth Orlando

• Located on a lush tropical campus, our flagship hospital, 1,368-bed AdventHealth Orlando
• Serves as the major tertiary facility for much of the Southeast, the Caribbean and South America
• AdventHealth Orlando houses one of the largest Emergency Departments and largest cardiac catheterization labs in the country
• We are already one of the busiest hospitals in the nation, providing service excellence to more than 32,000 inpatients and 125,000 outpatients each year
  
  

The role you’ll contribute\:

The Clinical Research Supervisor Non-RN 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 is able to function as a clinical study coordinator as needed and serves to train, mentor and develop the clinical study coordinators and research staff in the conduct of clinical research within the AdventHealth research enterprise at the institute level and may extend across multiple U.S. Division locations. Works closely with AHRI Managers and Leaders to facilitate the initiation through completion of clinical research studies in assigned areas. Provides day-to-day supervision and ongoing performance reviews 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\:

• Performs a variety of supervisory duties including, but not limited to, leading the Talent Acquisition process of applicant review and selection, team development and manages performance management of research team members including positive discipline and Talent Care discussions.
• Supervises day-to-day activity of the clinical research team within their assigned area, including oversight of team’s productivity and maintenance of personnel and staffing schedules as affected by research protocols at any given time.
• Supervises the delivery and delivers safe care with regard for the dignity and respect for all patients/participants.
• Serves as a service line expert and resource for the research team when barriers arise during day-to-day operations.
• Monitor and evaluate the quality and safety of clinical operations within their assigned area.
• Builds and maintains supportive relationships with each team member through rounding and frequently scheduled connections.
• Collaborates with operations manager, study intake, research services and external partners to foster a timely start up and smooth transition to assigned coordinator. This is inclusive, but not limited to, review of Medical Coverage Analysis, billing grids, and internal budgeting contribution for time and effort-based modeling. Ensures teams keep an open line of site for maintaining adequate inventory levels, ordering of approved equipment and supplies, maintenance of medical tools (biopsy needles, etc.) and clinical supply areas.
• Collaborates with AdventHealth Research Institute (AHRI)Operations Managers, Supervisors and Clinical Leaders within various inpatient and outpatient clinical settings to develop and implement processes that ensure workflow and scheduling are optimized for day-to-day operations.
• Under the direction of the Clinical Research Operations Manager, may develop and maintain Standard Operating Procedures (SOPs) and/or Work Instructions for the teams they supervise, and ensures clinical research operations teams follow AHRI processes and procedures.
• Manages the delivery of safe care with regard for the dignity and respect for all patients/participants.
• Provides guidance, inclusive of education, specialized training, and mentorship to promote growth for study team members, including those in new positions.
• Delivers effective and compliant clinical research study coordination as necessary, based on the needs of the department, including planning, organizing, and managing all activities related to clinical research protocols and execution of timelines, for industry-sponsored and investigator-initiated clinical trials.
• Serves in a supportive role for the preceptorship of new team members, which would be inclusive of monitoring the progress of each new team member and providing open communication to the Operational Manager for workflow planning.
• Participates in internal and/or external training programs to maintain certification(s).

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Hospitals and Health Care

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