Associate Clinical Research Coordinator - Comprehensive Cancer Center
About The Position
Coordinates non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with direction but does not have overall responsibility for these studies. Screens, enrolls, and recruits research participants. Coordinates schedules and monitors research activities and subject participation. Recognizes adverse events, protocol deviations, and other unanticipated problems and reports appropriately. Collects, abstracts, and enters research data. Performs administrative and regulatory duties related to the study as assigned. Some travel may be required. Protocol Development and Maintenance Activities Responsibilities 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. data collection booklets, use of CRU, etc.), and verification of content to meet institutional and federal standards; Institutional Review Board (IRB) submission; and communication with study sites and/or federal agencies regarding study status changes. Participates in other protocol development activities and executes other assignments as warranted and assigned.
Requirements
- Some travel may be required.
- Visa sponsorship is not available for this position.
- This position is not eligible for F-1 OPT STEM extension.
Responsibilities
- Coordinates non-therapeutic clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.
- May assist in complex studies with direction but does not have overall responsibility for these studies.
- Screens, enrolls, and recruits research participants.
- Coordinates schedules and monitors research activities and subject participation.
- Recognizes adverse events, protocol deviations, and other unanticipated problems and reports appropriately.
- Collects, abstracts, and enters research data.
- Performs administrative and regulatory duties related to the study as assigned.
- Ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics, and verification of content to meet institutional and federal standards.
- Institutional Review Board (IRB) submission.
- Communication with study sites and/or federal agencies regarding study status changes.
- Participates in other protocol development activities and executes other assignments as warranted and assigned.
Benefits
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
