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Oncology Clinical Trials Specialist

University of Vermont Health

Burlington, VTFull-time$25.78–40.67/hrSeen 1 day agoSeen in employer's feed 1 day ago

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At a glance

Compensation
$25.78–40.67/hr
Location
Burlington, VT
Schedule
Full-time
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

The Oncology Clinical Trials Specialist manages study startup timelines and operational requirements for cancer clinical trials, interpreting complex protocols and coordinating with regulatory, clinical, finance, and disease teams to ensure activation and alignment with strategic initiatives.

Skills & qualifications

RequiredNice to have

Skills

Study Startup ManagementProtocol InterpretationRegulatory NavigationCollaboration

Qualifications

Bachelor's in BS2+ Years ExperienceProfessional Certification

Full job description

Oncology Clinical Trials Specialist

Job Details

Job Ref:

R0089950

Category:

Research

Employment Type:

Full-Time

Health Care Partner:

University of Vermont Medical Center

Location:

University of Vermont Campus, Burlington, VT 05401

Department:

Hematology/Oncology II

Job Type:

Regular

Primary Shift:

Day

Hours:

Hours per Week:

40

Weekend Needs:

None

Pay Rate:

$25.78 - $40.67 per hour

This is a bargaining union position.

JOB SUMMARY:

The Oncology Clinical Trials Specialist is responsible for managing the study startup timeline and operations requirements for cancer clinical trials in conjunction with the clinical trials office regulatory, clinical, and finance teams and in alignment with department strategic initiatives. Interprets complex research protocols and identifies implicit and explicit items needed for trial activation. Navigates protocols through a complex activation system.

Works closely with Regulatory Affairs Supervisor, Clinical Research Supervisor, Regulatory Specialist, and disease teams to support a comprehensive study startup process, goals, and deadlines. Works proactively with various internal and external entities, clinic partners, departments, faculty members, and research collaborators to ensure protocol requirements can be met upon study activation.

EDUCATION:

BS required.

EXPERIENCE:

2+ years, professional certification preferred.

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