Study Coordinator

Apsida Life Science have partnered with a Global Pharmaceutical company looking for a Study Coordinator.
As the Study Coordinator, you will support the Principal Investigator and Clinical Research Associate by managing ongoing study tasks in accordance with the study protocol and guidance documents.
Responsibilities will include:
Assisting project teams with study-specific documentation and trial progress tracking by updating Clinical Trial Management SystemsFamiliarizing yourself with the CRA's role, attending site visits when appropriate, and working together to resolve queries.Ensuring adherence to ICH-GCP, the Research Governance Framework, the EU Clinical Trials Directive, and Spanish regulatory requirements while maintaining professional competence.Supporting the site teams to meet subject care requirements by following study schedules, protocols, and local clinical practices.Ensuring all relevant subject information is recorded, reported, and communicated.Delivering high-quality service in accordance with study protocols and Spanish regulations.Adapting to the dynamic nature of research visits and tasks as needed.Submitting Site Support Operative Report FormsThis role requires attention to detail, strong communication skills, and the ability to work within regulatory frameworks to ensure the success of clinical trial.
Experience: Previous role as a Study Coordinator or similar position at a research site, with current ICH-GCP certification (within the past year).
Minimum Qualifications: At least 2 years of experience as a Study Coordinator or Study Nurse on sponsored, global, multi-centre studies.

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