Remote Clinical Research Associate - Impactful Trials

Solventum in; Eagan (MN); Remote; USD 106,000 - 146,000; Full time

Job summary

Solventum, a healthcare company, seeks a Clinical Research Associate to join a remote team in the U.S. You will manage trial master file documentation, site visits, training, and regulatory compliance to ensure study quality and patient safety.

You will collaborate with the Clinical Project Manager and research partners, support device preparation and shipment tracking, and navigate state and federal regulations across clinical studies, while working in a flexible, remote-capable environment.

Qualifications

• Bachelor’s degree with 3 years clinical research experience including 2 years CRA monitoring.
• High School Diploma with 7 years clinical research experience including 5 years CRA monitoring.
• Experience with device preparation, site visits, regulatory compliance; familiarity with hospital or clinical settings; proficiency with Smartsheet/Microsoft 365.

Responsibilities

• Ensure TMF and regulatory file preparation and maintenance.
• Conduct pre-study site visits and select investigators.
• Perform site initiation visits and train site personnel on sponsor/regulatory requirements.
• Conduct site monitoring visits and ensure regulatory compliance across studies.
• Review case report forms and data queries for accuracy and completeness.
• Collaborate with the Clinical Project Manager and research partners.
• Assist with device preparation and shipment accountability.

Skills

Clinical research experience

Regulatory compliance knowledge

Communication skills

Education

Bachelor’s degree or higher

High School Diploma or GED

Tools

Smartsheet

Microsoft Copilot

Microsoft 365 applications

Job description

Solventum, a healthcare company, seeks a Clinical Research Associate to join a remote team in the U.S. You will manage trial master file documentation, site visits, training, and regulatory compliance to ensure study quality and patient safety.

You will collaborate with the Clinical Project Manager and research partners, support device preparation and shipment tracking, and navigate state and federal regulations across clinical studies, while working in a flexible, remote-capable environment.