Clinical Research Coordinator - Alzheimer's Disease Research

Responsibilities

• Independently coordinates complex clinical research protocols.
• Collaborates with research team to assess feasibility and manage research protocols.
• Ensures implementation of research protocols after IRB approval and provides information for progress reports.
• Screens, enrolls, and recruits research participants.
• Captures, monitors, and reports research data to maintain quality and compliance.
• Provides education/training for others within the department.
• Performs administrative and regulatory duties related to the study as appropriate.

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.
• One year of clinical research experience is preferred.
• A graduate or diploma from a study coordinator training program is preferred.
• Experience administering standardized cognitive tests is preferred.

Additional Qualifications

• Knowledge of medical terminology is preferred.
• Direct involvement in neuropsychometric testing and cognitive assessment procedures.

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.