Research Analyst

• Contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively
• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborating with investigators and site staff to facilitate smooth study conduct
• Performing data review and resolution of queries to maintain high-quality clinical data
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Clinical Research Associate

• Assess and identify the most suitable industry experts based on client objectives and project requirements
• Act as the primary liaison between clients and market specialists
• Conduct targeted research across industries, functions, and geographies
• Engage and recruit experts through structured outreach and relationship-building
• Develop core consulting capabilities, including stakeholder management, negotiation, time management, and professional communication

Market Research Associate

• Join Excelya, where **Audacity, Care, and Energy** define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.
• This role is an exciting opportunity to contribute to a dynamic, ambitious team in **Clinical Operations**. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.
• **Main Responsibilities:**
• - Perform monitoring of international clinical trials across Phases I–IV, ensuring protocol adherence and data integrity at investigational sites.
• - Guarantee scientific, regulatory, and technical quality through meticulous oversight and application of GCP and local regulatory standards.
• - Manage investigational product (IP) logistics including reconciliation, storage, dispensing, and inventory, with special focus on blinded/randomized protocols.
• Beyond that, you will also be able to:
• - Review and reconcile Investigator Site Files (ISF) with the Trial Master File (TMF) and ensure proper document archiving as per regulatory requirements.
• - Conduct routine monitoring and co-monitoring visits with CRAs to ensure source data verification, site performance, and resolution of deviations via CAPA processes.
• - Draft comprehensive monitoring visit reports in English and support audit readiness across all clinical sites.

Research Analyst jobs in Greece

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Clinical Research Associate

Market Research Associate

Clinical Research Associate