Associate Clinical Research Coordinator - Alzheimer's Disease Research - Limited Tenure
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. This position supports the Neurology AI program and Alzheimer's Disease Research Center. Candidates should possess strong technical proficiencies to assist study participants with troubleshooting issues with remote speech and language assessments. 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. This is a limited tenure position with an anticipated duration of two years, that may have the possibility of being turned into a regular ongoing position.
Requirements
- Strong technical proficiencies to assist study participants with troubleshooting issues with remote speech and language assessments.
Responsibilities
- Coordinates non-therapeutic clinical research protocols.
- Assists in complex studies with direction.
- Screens, enrolls, and recruits research participants.
- Coordinates schedules and monitors research activities and subject participation.
- Recognizes and reports adverse events, protocol deviations, and other unanticipated problems.
- Collects, abstracts, and enters research data.
- Performs administrative and regulatory duties related to the study.
- Manages protocol documents and processes, including editing, amendments, and proofing.
- Coordinates study logistics.
- Verifies content to meet institutional and federal standards.
- Submits to Institutional Review Board (IRB).
- Communicates with study sites and/or federal agencies regarding study status changes.
- Participates in other protocol development activities.
- 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
