Contract Clinical Research Associate

This is a fully remote position, open to applicants in Latvia.

📋 Description

• Conduct and document all forms of onsite monitoring visits.

• Execute CRF assessments, verify source documents, and resolve queries.

• Manage site communications and oversee operations.

• Act as a liaison for in-house support services and vendors.

• Update internal project teams on study advancements.

• Engage in feasibility studies.

• Assist the regulatory team in the preparation of documents for study submissions.

⛳️ Requirements

• Bachelor's degree in Life Sciences or an equivalent mix of education, training, and experience.

• Experience in independent monitoring in Latvia, ideally in a contractor or freelance capacity.

• Proficient in both English and Latvian.

• Skilled in using MS Office applications.

• Capable of planning, multitasking, and thriving in a dynamic team setting.

• Strong communication, collaboration, and problem-solving abilities.

• Willingness to travel.

• Possession of a valid driver's license.

🏝️ Benefits

• Flexible working arrangements.

• Comprehensive training programs.

• Opportunities for both personal and professional development.

• Competitive salary determined on an individual basis.