Research Supervisor - Oncology
AdventHealth University · Porter, ME
FULL-TIME
Posted Sep 18, 2026
68,328–127,088 a year
Job Description
Schedule:
Full time
Shift:
Day (United States of America)
Address:
2525 S DOWNING ST
City:
DENVER
State:
Colorado
Postal Code:
80210
Job Description:
• Manages the delivery of safe care with regard for the dignity and respect of all patients/participants.
• Supervises day-to-day activities of the clinical research team, including oversight of productivity and maintenance of personnel and staffing schedules.
• Leads the Talent Acquisition process, team development, and performance management of research team members.
• Serves as a service line expert and resource for the research team, addressing barriers during day-to-day operations.
• Builds and maintains supportive relationships with each team member through regular rounding and scheduled connections.
• Ensures teams maintain adequate inventory levels, order approved equipment and supplies, and maintain clinical supply areas.
• Collaborates with operations manager, study intake, research services, and external partners to ensure timely start-up and smooth transition to assigned coordinator.
• Monitors and evaluates the quality and safety of clinical operations within the assigned area.
• Develops and maintains Standard Operating Procedures (SOPs) and ensures clinical research operations teams follow established processes and procedures.
• Provides guidance, education, specialized training, and mentorship to promote growth for study team members.
• Delivers effective and compliant clinical research study coordination, including planning, organizing, and managing all activities related to clinical research protocols.
• Serves in a supportive role for the preceptorship of new team members, monitoring their progress and providing open communication to the Operational Manager.
• Performs other duties as assigned.
Knowledge, Skills, and Abilities:
• N/A
Education:
• Bachelor's [Required]
• Master's [Preferred]
Field of Study:
• in Healthcare Administration, Research, or related field
Work Experience:
• 2+ years of experience in clinical research [Required]
• 5+ clinical research experience with increasing people management responsibilities [Preferred]
Additional Information:
• An equivalent combination of education and relevant work experience may be considered in lieu of the stated degree requirement.
• Bachelors Degree AND 2+ years of experience in clinical research OR
• Associates Degree AND 4+ years of experience in clinical research or related field.
Licenses and Certifications:
• SOCRA Certified Clinical Research Professional (CCRP) [Preferred] OR ACRP Certified Clinical Research Coordinator (CCRC) [Preferred]
• Basic Life Support - CPR Cert (BLS) [Required]
• Advanced Cardiac Life Support Cert (ACLS) [Preferred]
Physical Requirements: (Please click the link below to view work requirements)
Physical Requirements - https://tinyurl.com/msy4mja2
Pay Range:
$68,328.00 - $127,088.00
Full time
Shift:
Day (United States of America)
Address:
2525 S DOWNING ST
City:
DENVER
State:
Colorado
Postal Code:
80210
Job Description:
• Manages the delivery of safe care with regard for the dignity and respect of all patients/participants.
• Supervises day-to-day activities of the clinical research team, including oversight of productivity and maintenance of personnel and staffing schedules.
• Leads the Talent Acquisition process, team development, and performance management of research team members.
• Serves as a service line expert and resource for the research team, addressing barriers during day-to-day operations.
• Builds and maintains supportive relationships with each team member through regular rounding and scheduled connections.
• Ensures teams maintain adequate inventory levels, order approved equipment and supplies, and maintain clinical supply areas.
• Collaborates with operations manager, study intake, research services, and external partners to ensure timely start-up and smooth transition to assigned coordinator.
• Monitors and evaluates the quality and safety of clinical operations within the assigned area.
• Develops and maintains Standard Operating Procedures (SOPs) and ensures clinical research operations teams follow established processes and procedures.
• Provides guidance, education, specialized training, and mentorship to promote growth for study team members.
• Delivers effective and compliant clinical research study coordination, including planning, organizing, and managing all activities related to clinical research protocols.
• Serves in a supportive role for the preceptorship of new team members, monitoring their progress and providing open communication to the Operational Manager.
• Performs other duties as assigned.
Knowledge, Skills, and Abilities:
• N/A
Education:
• Bachelor's [Required]
• Master's [Preferred]
Field of Study:
• in Healthcare Administration, Research, or related field
Work Experience:
• 2+ years of experience in clinical research [Required]
• 5+ clinical research experience with increasing people management responsibilities [Preferred]
Additional Information:
• An equivalent combination of education and relevant work experience may be considered in lieu of the stated degree requirement.
• Bachelors Degree AND 2+ years of experience in clinical research OR
• Associates Degree AND 4+ years of experience in clinical research or related field.
Licenses and Certifications:
• SOCRA Certified Clinical Research Professional (CCRP) [Preferred] OR ACRP Certified Clinical Research Coordinator (CCRC) [Preferred]
• Basic Life Support - CPR Cert (BLS) [Required]
• Advanced Cardiac Life Support Cert (ACLS) [Preferred]
Physical Requirements: (Please click the link below to view work requirements)
Physical Requirements - https://tinyurl.com/msy4mja2
Pay Range:
$68,328.00 - $127,088.00
Additional Details
- City
- Porter
- State
- Maine
- Country
- US
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