Clinical Research Associate

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

📋 Description

• Conduct qualification, site initiation, monitoring, and termination visits at designated clinical sites.

• Prepare visit and contact reports.

• Establish and nurture relationships with clinical sites and their personnel.

• Address and resolve inquiries and issues from sites as the primary point of contact.

• Ensure study integrity and employ problem-solving skills effectively.

• Review trial performance while safeguarding the rights and well-being of human subjects.

• Collaborate with clinical sites to develop patient recruitment strategies to meet enrollment timelines.

• Maintain compliance with SOPs, protocols/amendments, GCP, and relevant regulatory requirements.

• Assess the quality and integrity of reported data, site efficacy, and drug accountability.

• Supervise the completeness and quality of regulatory documentation.

• Execute site document verification.

• Oversee site quality and delivery from identification through to close-out.

⛳️ Requirements

• Experience in Site Management or comparable experience in clinical research.

• Understanding of clinical trial methodologies and terminology.

• Exceptional interpersonal, verbal, and written communication abilities.

• Proficiency in Finnish.

• Conversational proficiency in Swedish.

• A degree, preferably in biological sciences, pharmacy, or another health-related field, or an equivalent nursing qualification or relevant experience.

• Capability to perform clinical site visits and manage site relationships effectively.

• Knowledge of SOPs, protocols/amendments, GCP, and relevant regulatory standards.

• Experience or ability to assess clinical data quality, site efficacy, and drug accountability.

• Experience or ability to monitor regulatory documentation and carry out site document verification.

🏝️ Benefits

• Access to world-class technology and training tailored to individual experience.

• Reduced travel requirements and a lower protocol load compared to industry standards.

• Bonus incentive program.

• Opportunities to work across multiple therapeutic areas.

• Career advancement possibilities.

• Regular performance discussions and evaluations.

• Management support for professional growth.

• Potential to progress into senior CRA roles, line management, Quality, Project Leadership, or other positions.

• An open team environment fostering regular clinical research discussions and knowledge sharing.