Contract Clinical Research Associate

About the role

Contract Clinical Research Associate role, remote in Latvia at approximately 0.5 FTE. Responsibilities include onsite monitoring, CRF and source document review, query resolution, site and vendor management, feasibility research, and regulatory submission support. Requires a Life Sciences college/university degree or equivalent education, training and experience, independent monitoring experience in Latvia, English and Latvian proficiency, MS Office skills, travel ability, and a valid driver’s license.

Key requirements

• • College/University degree in Life Sciences or an equivalent combination of education, training & experience
• • Required skills: Independent monitoring experience in Latvia, Clinical trial monitoring, CRF review, Source document verification, Query resolution, Site communication and management, Vendor communication, Study progress reporting, Feasibility research, Regulatory submission document preparation, MS Office applications, Planning and multitasking, Communication, Collaboration, Problem-solving, Ability to travel
• • Required languages: English, Latvian
• • Professional registration/licence (Latvia)

Opportunity details

• • Workplace: Remote
• • Employment: Contract
• • Posted: Oct 20, 2026
• • Original advert language: English

Full vacancy

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