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Clinical Operations Manager
Job Location:
Job Location:
Chapel Hill, NC - USA
Monthly Salary:
Not provided by the employer
Monthly Salary:
Posted:
3 June 2026 (30+ days ago)
Posted:
Application Deadline:
31 August 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Position Summary
The Clinical Operations Manager provides oversight and management of a large number of clinical research staff to ensure safe compliant efficient and effective conduct of oncology clinical trials. This position provides expert level knowledge in clinical trial practices and regulations. This position works under the direct supervision of the Assistant Director of Clinical Research Operations to ensure safe implementation of oncology clinical trials. The Clinical Operations Manager manages clinical research staff assigned to various disease teams within the Clinical Protocol Office ( CPO ) providing daily management/supervision resource and effort allocation overseeing research compliance and data integrity and assisting in strategic planning and operational support. This position creates and champions a collaborative and positive relationship dynamic with internal staff and external agencies/organizations.
Required Qualifications Competencies And Experience
Advanced knowledge of ICH GCP Federal Regulations and Guidelines and ability to follow established regulations procedures and protocols; clinical research experience; Experience in interviewing/hiring process and performance management; Possess strong decision-making skills and the ability to problem solve and troubleshoot issues; Strong organizational skills with the ability to manage large volumes of information; High level of accuracy and attention to detail; High level of comfort with technology; Strong computer skills; Ability to gather data and document procedures; Ability to plan work and coordinate multiple projects; Ability to contribute to preparation and delivery of reports trainings and SOPs; Customer oriented and ability to work within build and lead a team; Exceptional interpersonal skills and excellent verbal and written communication skills in daily interactions with the ability to interpret and apply UNC policies and federal state and local regulations; Ability to work on evenings weekends and/or holidays occasionally required.
Preferred Qualifications Competencies And Experience
Therapeutic clinical trial coordination experience involving drugs and/or devices to include work in oncology; SOCRA / ACRP certification; Supervisory experience; Experience in Phase I II and III clinical research; Experience navigating medical records and data extraction; Experience leading a large team.
The Clinical Operations Manager provides oversight and management of a large number of clinical research staff to ensure safe compliant efficient and effective conduct of oncology clinical trials. This position provides expert level knowledge in clinical trial practices and regulations. This position works under the direct supervision of the Assistant Director of Clinical Research Operations to ensure safe implementation of oncology clinical trials. The Clinical Operations Manager manages clinical research staff assigned to various disease teams within the Clinical Protocol Office ( CPO ) providing daily management/supervision resource and effort allocation overseeing research compliance and data integrity and assisting in strategic planning and operational support. This position creates and champions a collaborative and positive relationship dynamic with internal staff and external agencies/organizations.
Required Qualifications Competencies And Experience
Advanced knowledge of ICH GCP Federal Regulations and Guidelines and ability to follow established regulations procedures and protocols; clinical research experience; Experience in interviewing/hiring process and performance management; Possess strong decision-making skills and the ability to problem solve and troubleshoot issues; Strong organizational skills with the ability to manage large volumes of information; High level of accuracy and attention to detail; High level of comfort with technology; Strong computer skills; Ability to gather data and document procedures; Ability to plan work and coordinate multiple projects; Ability to contribute to preparation and delivery of reports trainings and SOPs; Customer oriented and ability to work within build and lead a team; Exceptional interpersonal skills and excellent verbal and written communication skills in daily interactions with the ability to interpret and apply UNC policies and federal state and local regulations; Ability to work on evenings weekends and/or holidays occasionally required.
Preferred Qualifications Competencies And Experience
Therapeutic clinical trial coordination experience involving drugs and/or devices to include work in oncology; SOCRA / ACRP certification; Supervisory experience; Experience in Phase I II and III clinical research; Experience navigating medical records and data extraction; Experience leading a large team.
Required Experience:
Staff IC
About Company
The University of North Carolina at Chapel Hill, the nation’s first public university, is a global higher education leader known for innovative teaching, research and public service. A member of the prestigious Association of American Universities, Carolina regularly ranks as the best ... View more
