Clinical Research Coordinator - Comprehensive Cancer Center

Clinical Research Coordinator - Comprehensive Cancer Center jobs in United States

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50+ applicants

Original Job Post

Mayo Clinic

Clinical Research Coordinator - Comprehensive Cancer Center

$27.99/hr - $41.98/hr

92

STRONG MATCH

Experience Level

100

Skill

99

Industry Exp.

Responsibilities

Independently coordinate complex (i.e. interventional, therapeutic greater than minimal risk) clinical research protocols with minimal direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines

Collaborate with research team to assess feasibility and management of research protocols

Ensure implementation of research protocols after IRB approval and provide information as appropriate for progress reports

Screen, enroll, and recruit research participants

Coordinate schedules and monitor research activities and subject participation

Identify, review, and report adverse events, protocol deviations, and other unanticipated problems appropriately

Manage, monitor, and report research data to maintain quality and compliance

Provide education/training for others within the department

Perform administrative and regulatory duties related to the study as appropriate

Perform Protocol Development and Maintenance Activities Responsibilities, which may include, but are not limited to: ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics (i.e. blood collection kits, data collection booklets, use of CRU, etc.), and verification of content to meet institutional and federal standards; communication with study sites and/or federal agencies regarding study status changes; Federal and Institutional Review Board (IRB) document preparation and submission; and provides consultative expertise regarding regulatory and policy requirements

Accurately apply investigators' scientific data into a cohesive format for the protocol document and associated procedures that are consistent with internal and external policies and regulatory requirements

Participate in other protocol development activities and execute other assignments as warranted and assigned

Preferred

Graduate or diploma from a study coordinator training program is preferred

One year of clinical research experience is preferred

Medical terminology course is preferred

Benefits

Benefits Eligible: Yes

Medical: Multiple plan options.

Dental: Delta Dental or reimbursement account for flexible coverage.

Vision: Affordable plan with national network.

Pre-Tax Savings: HSA and FSAs for eligible expenses.

Retirement: Competitive retirement package to secure your future.

Glassdoor

3.7

MayoClinic is a nonprofit medical practice and medical research group focused on integrated health care, education, and research.

Rochester, Minnesota, USA

https://www.mayoclinic.org

Late Stage

Total Funding

$399.05M

Key Investors

The ALS Association

National Institute of Neurological Disorders and Stroke

American Heart Association

2025-12-04

Grant· $0.95M

2024-09-24

Grant· $12M

2023-07-26

Grant

Leadership Team

Gianrico Farrugia

President and CEO

James Rogers

CEO of Digital Pathology

Recent News

Qualifications

HS Diploma with at least 5 years of clinical research coordination/related experience OR

Associate's degree/college Diploma/Certificate Program with at least 3 years of experience OR

Associate's in Clinical Research from an accredited academic institution without experience OR

Bachelor's with at least 1 year of experience or completion of a Mayo Clinic-sponsored clinical research internship in lieu of 1 year of experience

Experience should be in the clinical setting or related experience

Graduate or diploma from a study coordinator training program is preferred

One year of clinical research experience is preferred

Medical terminology course is preferred

Bachelor's with at least 1 year of experience or completion of a Mayo Clinic-sponsored clinical research internship in lieu of 1 year of experience.

Required skills

Clinical Research Coordination, Interventional Clinical Research Protocols, Therapeutic Clinical Research Protocols, Regulatory Compliance, Institutional Review Board (IRB) Processes, Research Participant Recruitment, Adverse Event Reporting, Clinical Data Management, Protocol Development, Medical Terminology

Preferred skills

One year of clinical research experience is preferred, Medical terminology course is preferred

Experience

1+ years