Field Clinical Research Lead – Trials & Compliance

MED Medtronic Inc; Minnesota; Remote; USD 129,000 - 170,000; Full time

Benefits offered by this job

Health, Dental and Vision Insurance

401(k) with company match

Paid time off

Job summary

Medtronic, Inc. is seeking a Sr. Field Clinical Research Specialist in Minneapolis, MN to lead field-based responsibilities for clinical trial site management, case coverage, and data tracking.

You will ensure regulatory compliance and drive patient recruitment strategies, with extensive travel up to 75% in the Chicago metro and surrounding regions. Responsibilities include coordinating start-up, initiation, monitoring, and close-out, plus CAPA, IRB submissions, and CTMS usage.

Qualifications

• Master’s degree in Biological Science, Nursing, Biomedical Engineering, or Biotechnology.
• Two years’ experience in clinical research or related field.
• Experience with GCP and regulatory guidelines for trials.

Responsibilities

• Lead field-based oversight of clinical trials with regulatory adherence.
• Coordinate study start-up, initiation, monitoring, and close-out.
• Develop ICF, protocol, and amendments; oversee site staff training.

Skills

GCP compliance

Clinical trial design

Site monitoring

Regulatory knowledge

Travel readiness

Education

Master’s degree in Biological Science or related field

Tools

CTMS

Veeva Vault CTMS

Oracle Siebel CTMS

Salesforce

Job description

Medtronic, Inc. is seeking a Sr. Field Clinical Research Specialist in Minneapolis, MN to lead field-based responsibilities for clinical trial site management, case coverage, and data tracking.

You will ensure regulatory compliance and drive patient recruitment strategies, with extensive travel up to 75% in the Chicago metro and surrounding regions. Responsibilities include coordinating start-up, initiation, monitoring, and close-out, plus CAPA, IRB submissions, and CTMS usage.