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

📋 Description

• Independently organize, execute, and follow up on pre-study preparations, site initiation, routine monitoring, and close-out visits.

• Supervise the performance of study sites, including monitoring recruitment progress, and provide continuous support to the sites.

• Analyze eCRF data, timelines, and queries; identify and report any protocol deviations.

• Maintain effective communication with project management and sponsors.

• Work collaboratively across departments with medical, project management, quality management, and data management teams.

⛳️ Requirements

• A degree in a scientific or medical field, or completed vocational training in a pertinent healthcare or medical discipline.

• Additional training in clinical research or certification as a Clinical Research Associate (CRA).

• Several years of experience as a Clinical Research Associate.

• Strong understanding of Good Clinical Practice (GCP), ICH guidelines, and clinical research processes.

• Proficient in both written and spoken Swedish and English.

• Willingness to travel domestically and internationally as necessary.

• Extensive experience in Medical Device studies and knowledge of ISO14155.

🏝️ Benefits

• Opportunities for personal and professional development in a fulfilling environment.

• Become part of a team that prioritizes collaboration, quality, and making a positive impact.

• Core values of Trust, Quality, Passion, Flexibility, and Sustainability.