Senior Clinical Research Associate – Freelance

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

📋 Description

• Oversee both on-site and remote clinical trials in alignment with TFS and/or sponsor standards.

• Conduct all necessary monitoring activities at study sites to evaluate and ensure the safety of subjects, as well as the integrity and quality of data.

• Ensure the protection of study participants by adhering to informed consent procedures and protocol requirements that comply with relevant regulations.

• Assess CRFs (electronic or paper) and subject source documentation for validity and accuracy.

• Confirm the proper management and accountability of Investigational Product.

• Promptly report actions taken during monitoring visits in the Monitoring Visit Report, which includes findings, corrective and preventive actions already implemented, and updates to applicable tracking systems as necessary; escalate observed deficiencies and issues as needed.

• Conduct Close-out monitoring visits in Ukraine.

⛳️ Requirements

• Bachelor’s Degree, ideally in life sciences or nursing, or an equivalent qualification.

• More than 1 year of relevant clinical experience or a pertinent academic background in clinical trials or clinical development activities.

• Strong understanding of Good Clinical Practice regulations and ICH guidelines.

• Proficient in English and Ukrainian.

🏝️ Benefits

• We offer opportunities for personal and professional development in a fulfilling environment.

• You will be part of a team that prioritizes collaboration, quality, and making a positive impact on patients' lives.

• Our core values of Trust, Quality, Passion, Flexibility, and Sustainability influence our decisions and shape our organizational culture.