Experienced CRA

Thermo Fisher Scientific · Stockholm, Sweden

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Clinical OperationsFull timeCompany career page

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Role summary

Thermo Fisher Scientific (PPD) seeks an experienced Clinical Research Associate to conduct remote and on-site monitoring of investigational sites across clinical trials. The role involves ensuring protocol compliance, data accuracy, and regulatory adherence while managing site relationships and documentation.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Phenom, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-03 (originally posted 2026-10-03). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

Bachelor's degree in life sciences or registered nursing certification
3+ years experience as clinical research monitor in pharma, biotech, or CRO
Valid driver's license
Strong knowledge of ICH-GCP guidelines and applicable regulations
Critical thinking and root cause analysis skills for problem-solving
Medical/therapeutic area knowledge and medical terminology proficiency

What you'll be doing

Conduct risk-based monitoring visits to investigational sites and assess protocol compliance
Review source documents, case report forms, and investigational product records for accuracy
Document deficiencies in monitoring reports and escalate issues to clinical management for resolution
Initiate and close out clinical trial sites while ensuring essential regulatory documents are complete
Provide trial status updates and maintain study systems per project specifications

Privacy & handoff

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What RoleLantern checked

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Date posted1 day ago

Last source checkToday

Salary listedNeeds clarity

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