Hybrid Clinical Research Coordinator - Protocol & Compliance

Mayo Clinic; Rochester (MN); Hybrid; USD 39,000 - 58,000; Full time

Benefits offered by this job

Hybrid work nearby Rochester

Job summary

Mayo Clinic in Rochester, MN seeks a clinical research coordinator to independently manage complex protocols and ensure regulatory compliance. The role involves screening, enrolling, and recruiting participants, coordinating study logistics, and providing training within the department. Travel may be required, and a hybrid on-site arrangement is offered near Rochester.

Exemption status is Nonexempt. Schedule is Full Time with 64 hours per pay period. Visa sponsorship is not available.

Qualifications

• HS Diploma with at least 5 years of clinical research coordination/related experience or
• Associate's degree with at least 3 years of experience or completion of Mayo Clinic internship in lieu of 1 year, as applicable
• Experience should be in a clinical research setting or related field

Responsibilities

• Coordinate complex clinical research protocols with minimal direction in compliance with regulatory laws
• Screen, enroll, and recruit research participants; monitor subject participation and data quality
• Manage protocol development, regulatory duties, and study logistics; travel may be required

Skills

Clinical research coordination

Regulatory compliance

IRB processes

Education

HS Diploma

Associate's degree

Bachelor's degree

Clinical Research internship

Job description

Mayo Clinic in Rochester, MN seeks a clinical research coordinator to independently manage complex protocols and ensure regulatory compliance. The role involves screening, enrolling, and recruiting participants, coordinating study logistics, and providing training within the department. Travel may be required, and a hybrid on-site arrangement is offered near Rochester.

Exemption status is Nonexempt. Schedule is Full Time with 64 hours per pay period. Visa sponsorship is not available.