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Clinical Operations Manager

University of North Carolina- Chapel Hill

NC-Chapel-Hill, NCJobNo compensation foundTracked 2mo agoSeen in employer's feed today

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At a glance

Compensation
No compensation found
Location
NC-Chapel-Hill, NC
Work Authorization
Not specified

Requirements

Credentials this posting asks for.

SOCRA / ACRP Certification

Job overview

The Clinical Operations Manager oversees a large clinical research staff, ensuring safe, compliant, and efficient conduct of oncology trials. Reporting to the Assistant Director, they manage resources, supervise teams, maintain data integrity, and support strategic planning while fostering collaborative relationships with internal and external partners.

Skills & qualifications

RequiredNice to have

Skills

ICH GCP KnowledgeFederal Regulations KnowledgeClinical Research ExperienceInterviewing and HiringPerformance ManagementDecision MakingProblem SolvingStrong Organizational SkillsAccuracyAttention to DetailTechnology ComfortComputer SkillsData GatheringProject PlanningMulti-Project CoordinationReport PreparationTraining DeliverySOP DevelopmentCustomer OrientationTeam LeadershipInterpersonal SkillsVerbal CommunicationWritten CommunicationPolicy InterpretationEvening Weekend Availability

Qualifications

Therapeutic Clinical Trial Coordination Experience in OncologySOCRA / ACRP CertificationSupervisory ExperiencePhase I, II, and III Clinical Research ExperienceMedical Records Navigation and Data Extraction ExperienceLarge Team Leadership Experience

Full job description

Employment Type: Permanent Staff (EHRA NF)

Vacancy ID: NF0009791

Salary Range: Salary commensurate with qualifications

Position Summary/Description:

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.

Education 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.

Essential Skills:

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.

AA/EEO Statement:

The University is an equal opportunity employer and welcomes all to apply without regard to age, color, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex, or sexual orientation. We encourage all qualified applicants to apply, including protected veterans and individuals with disabilities.

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