Clinical Trial Coordinator

Apsida Life Science is seeking a highly skilled Clinical Trial Coordinator to support the success of our global pharmaceutical partnerships.

• Study Management: Assist project teams with study-specific documentation and trial progress tracking by updating Clinical Trial Management Systems.
• Clinical Research Support: Familiarize yourself with the CRA's role, attend site visits when appropriate, and work together to resolve queries.
• Regulatory Compliance: Ensure adherence to ICH-GCP, the Research Governance Framework, the EU Clinical Trials Directive, and Spanish regulatory requirements while maintaining professional competence.
• Subject Care: Support the site teams to meet subject care requirements by following study schedules, protocols, and local clinical practices.
• Reporting and Communication: Ensure all relevant subject information is recorded, reported, and communicated.
• Service Delivery: Deliver high-quality service in accordance with study protocols and Spanish regulations.
• Adaptability: Adapt to the dynamic nature of research visits and tasks as needed.
• Reporting and Compliance: Submit Site Support Operative Report Forms.

• Experience: Previous role as a Study Coordinator or similar position at a research site, with current ICH-GCP certification (within the past year).
• Qualifications: At least 2 years of experience as a Study Coordinator or Study Nurse on sponsored, global, multi-centre studies.