Clinical Research Specialist, Cardiology Trials (Onsite)

Medtronic; Mounds View (MN); On-site; USD 83,000 - 125,000; Full time

Job summary

Medtronic is seeking a Clinical Research Specialist in the Interventional Cardiology Therapies ICT unit, based in Mounds View, MN. The role focuses on study execution, site management, regulatory adherence, and collaboration with the Clinical Study Manager to meet SOP and GCP standards.

The position requires a bachelor’s degree with 2+ years of clinical research experience or an advanced degree with 0 years. Strong knowledge of GCP, cross-functional teamwork, and site coordination is preferred.

Qualifications

• Bachelor's degree and a minimum of 2 years of clinical research experience or an advanced degree with 0 years of experience.
• Experience in Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials.
• Experience managing multiple clinical research sites with proven results in study execution and clinical operations.

Responsibilities

• Review and approve documents for study start and site activation; monitor ongoing validity.
• Perform site initiation, issue resolution, and site closure activities.
• Provide training for clinical study sites to assure data integrity and protocol compliance.

Skills

Clinical research

Site management

Regulatory compliance

Cross-functional coordination

Education

Bachelor's degree + clinical research exp

Advanced degree (MS/PhD)

Tools

GCP

Regulatory guidelines

Job description

Medtronic is seeking a Clinical Research Specialist in the Interventional Cardiology Therapies ICT unit, based in Mounds View, MN. The role focuses on study execution, site management, regulatory adherence, and collaboration with the Clinical Study Manager to meet SOP and GCP standards.

The position requires a bachelor’s degree with 2+ years of clinical research experience or an advanced degree with 0 years. Strong knowledge of GCP, cross-functional teamwork, and site coordination is preferred.