Freelance Clinical Research Associate

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

📋 Description

• Oversee all elements of study site management for designated clinical trials

• Execute feasibility assessments for countries and sites

• Manage site administration and monitoring in accordance with Dokumeds and Sponsor SOPs, legal standards, and ICH-GCP Guidelines

• Perform site initiation, routine monitoring, and close-out visits

• Prepare and submit documentation to Ethics Committees and Regulatory Authorities

• Aid in the management of site contracts

• Guarantee data quality and integrity

• Ensure adherence to SOPs and regulatory standards

• Facilitate the timely and budget-compliant completion of studies

• Maintain comprehensive study files

⛳️ Requirements

• Bachelor's degree in medicine, pharmacy, nursing, or a life science discipline

• Minimum of 2 years of prior on-site monitoring experience with a CRO or pharmaceutical company

• Prior experience in preparing and submitting documents to Ethics Committees / Regulatory Authorities

• Freelancing experience is considered a plus

• Exceptional written, verbal, and presentation abilities

• Proficiency in both English and local languages

• Strong attention to detail and a solid understanding of high-quality scientific standards

• Values such as honesty, integrity, loyalty, accountability, mutual trust, and a strong sense of teamwork

• Ability to think critically and devise innovative, practical solutions

• Capacity to adapt quickly, manage risks, and embrace change

• Valid driver's license and willingness to travel

• CV must be submitted in English

🏝️ Benefits

• A position that presents daily exciting challenges within a highly skilled and international team

• A work environment that is friendly to employees

• Competitive salary package

• Opportunities for professional growth and learning in the Clinical Research field

• Financial, workforce, and corporate stability

• A supportive and collaborative community