Clinical Research Coordinator: Protocols, IRB & Participants

Socket.dev; Eau Claire (WI); On-site; USD 65,000 - 90,000; Full time

Job summary

Mayo Clinic seeks a qualified professional to independently coordinate complex clinical research protocols with minimal direction, ensuring compliance with regulatory laws and guidelines.

You will screen, enroll and recruit participants, manage data quality and reporting, support protocol development, and collaborate with study sites, IRB filings, and federal agencies. Some travel may be required. Excellent training and professional growth opportunities are available at Mayo Clinic.

Qualifications

• Clinical research coordination experience preferred.
• Familiarity with IRB processes and regulatory standards.

Responsibilities

• Coordinates complex clinical research protocols with minimal PI direction.
• Screens, enrolls, and recruits research participants.
• Identifies, reviews, and reports adverse events and protocol deviations.
• Manages and audits study data to maintain quality and compliance.
• Provides education and training for department staff.
• Performs administrative duties related to the study and regulatory compliance.
• Some travel may be required.

Job description

Mayo Clinic seeks a qualified professional to independently coordinate complex clinical research protocols with minimal direction, ensuring compliance with regulatory laws and guidelines.

You will screen, enroll and recruit participants, manage data quality and reporting, support protocol development, and collaborate with study sites, IRB filings, and federal agencies. Some travel may be required. Excellent training and professional growth opportunities are available at Mayo Clinic.