Remote Cardiac Field Clinical Lead – Chicago

Medtronic; Minneapolis (MN); Remote; USD 129,000 - 170,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401(k) matching

Life insurance

Paid time off

Tuition assistance

Employee Stock Purchase Plan

Job summary

Medtronic is seeking a Sr. Field Clinical Research Specialist to manage field-based clinical trial activities in the Minneapolis area. You will coordinate start-up, site initiation, monitoring, and close-out while ensuring regulatory compliance and data integrity across trials.

Responsibilities include ICF/protocol development, patient recruitment strategies, and SAE/AE reporting, with travel up to 75% and remote work from a Chicago metro area home office as needed.

Qualifications

• Master’s degree in Biological Science, Nursing, Biomedical Engineering, or Biotechnology with two years of clinical research experience.
• Experience with GCP, regulatory compliance guidelines, and FDA/ICH guidelines.
• Familiarity with CTMS systems (Veeva Vault CTMS, Oracle Siebel CTMS) and Salesforce.

Responsibilities

• Lead field-based responsibilities for trial site management, case coverage, and data tracking.
• Coordinate start-up, site initiation, monitoring, and close-out activities.
• Develop and review ICF, protocol, and amendments; drive patient recruitment and retention strategies.
• Ensure SDV, AE/SAE reporting, and regulatory compliance across trials.

Skills

GCP Compliance

Regulatory Compliance

Clinical Trial Design

CTMS

IRB Submission

Site Monitoring

SDV

Patient Recruitment

SAE/AE Reporting

Education

Master’s degree in Biological Science/Nursing/Biomedical Engineering

Tools

Veeva Vault CTMS

Oracle Siebel CTMS

Salesforce

Job description

Medtronic is seeking a Sr. Field Clinical Research Specialist to manage field-based clinical trial activities in the Minneapolis area. You will coordinate start-up, site initiation, monitoring, and close-out while ensuring regulatory compliance and data integrity across trials.

Responsibilities include ICF/protocol development, patient recruitment strategies, and SAE/AE reporting, with travel up to 75% and remote work from a Chicago metro area home office as needed.