Remote Clinical Research Associate | Impactful Trials

SOLVENTUM; Oregon; Hybrid; USD 106,000 - 146,000; Full time

Benefits offered by this job

Medical, Dental & Vision

Health Savings Accounts

Health Care & Dependent Care Flexible;

Disability Benefits

Life Insurance

Voluntary Benefits

Paid Absences

Retirement Benefits

Job summary

Solventum is seeking a Clinical Research Associate (CRA) to join our remote team in the United States. You will monitor trials, ensure TMF and regulatory file integrity, and collaborate with cross-functional teams to drive compliant study execution.

Required qualifications include a bachelor’s degree with CRA experience or a high school diploma with extensive CRA background. Travel up to 75% is noted, with strong emphasis on regulatory knowledge and data accuracy.

Qualifications

• Bachelor-level plus 3 years of clinical research/medical device experience, including 2 years in CRA monitoring.
• High School Diploma plus 7 years in clinical research/medical device fields, including 5 years CRA monitoring experience.

Responsibilities

• Ensure preparation, collection, and distribution of TMF documents and regulatory files at sites.
• Conduct pre-study site visits and assist in investigator/site selection.
• Train site personnel on sponsor and regulatory requirements for study conduct.
• Perform site monitoring visits and address regulatory/compliance issues.
• Review source documents and CRFs for accuracy and completeness; remediate deficiencies.
• Investigate CRF queries and changes; coordinate data clarification as needed.
• Collaborate with Clinical Project Manager and cross-functional teams.
• Assist with device preparation, shipment coordination, and accountability records.

Skills

Clinical research

Regulatory knowledge

Site monitoring

Education

Bachelor's degree + 3 years CRA experience

High School Diploma + 7 years CRA experience

Tools

Smartsheet

Microsoft Copilot

Microsoft 365

Job description

Solventum is seeking a Clinical Research Associate (CRA) to join our remote team in the United States. You will monitor trials, ensure TMF and regulatory file integrity, and collaborate with cross-functional teams to drive compliant study execution.

Required qualifications include a bachelor’s degree with CRA experience or a high school diploma with extensive CRA background. Travel up to 75% is noted, with strong emphasis on regulatory knowledge and data accuracy.