Clinical Research Supervisor: Lead Patient-Centric Trials

Mayo Foundation for Medical Education and Research; Rochester (MN); On-site; USD 88,000 - 124,000; Full time

Benefits offered by this job

Medical options

Dental coverage

Vision plan

HSA/FSAs for eligible expenses

Retirement package

Job summary

Mayo Clinic in Rochester seeks a Clinical Research Supervisor to oversee daily clinical operations and guide allied health staff in delivering patient-focused care. You will coordinate protocol implementation, ensure regulatory compliance, and participate in budget planning.

Join a team that values leadership, continuous quality improvement, and collaborative problem solving, with opportunities for professional growth in a renowned research environment.

Qualifications

• Bachelor's degree; 3–5 years clinical research experience.
• Supervisory or leadership experience in healthcare setting.
• SOCRA or ACRP certification preferred.

Responsibilities

• Oversee day-to-day clinical operations of the designated work unit.
• Coordinate activities implementing research protocols and ensure quality patient care.
• Interface with departments to integrate clinical practice and investigate new programs.
• Ensure compliance with regulatory agencies and Good Clinical Practice.
• Conduct budget planning and compliance.
• Recruit and retain competent staff; mentor and participate in committees.
• Collaborate with Research Administration to develop programs and policies.
• Demonstrate leadership with strong communication and problem-solving to maintain productivity.

Skills

Leadership

Problem solving

Communication skills

Autonomy

Technology literacy

Education

Bachelor's degree

Associate degree + 7 years research experience

High school diploma + 9 years research experience

SOCRA or ACRP certification

Tools

Word

Excel

Database experience

Job description

Mayo Clinic in Rochester seeks a Clinical Research Supervisor to oversee daily clinical operations and guide allied health staff in delivering patient-focused care. You will coordinate protocol implementation, ensure regulatory compliance, and participate in budget planning.

Join a team that values leadership, continuous quality improvement, and collaborative problem solving, with opportunities for professional growth in a renowned research environment.