Research Analyst

• Design, plan, and oversee clinical evaluation and research studies
• Prepare and write clinical study protocols, patient tracking forms, and related study documents
• Conduct registered and unregistered clinical studies for products addressing unmet medical needs and/or demonstrating commercial potential
• Oversee and interpret clinical investigation results to support new submissions for medical devices, drugs, or consumer healthcare products
• Manage and resolve operational aspects of clinical trials in collaboration with cross-functional project teams, ensuring compliance with standard operating procedures, Good Clinical Practice (GCP), and applicable country-specific regulations
• Support clinical trial planning activities, including budget preparation, clinical procurement operations, and site and vendor selection where needed
• Represent Medtronic from a clinical research perspective within the country or region, building effective internal and external partnerships, collecting feedback from customers and local authorities, and leading local evidence dissemination and outreach efforts.

Senior Clinical Research Specialist

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations

Senior Clinical Research Associate

• Conduct site initiation visits, monitoring visits, and close-out visits.
• Ensure site compliance with study protocols, ICH-GCP guidelines, and applicable regulations.
• Communicate effectively with study sites to facilitate the trial process and address any issues that arise.
• Review and verify study-related documents and data for accuracy and completeness.
• Monitor patient safety and data integrity throughout the study.
• Assist in preparing for audits and regulatory inspections.
• Provide regular updates to project managers and stakeholders about site progress and challenges.

Clinical Research Associate – Oncology

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions

Clinical Research Associate II

• Contributing to clinical trial monitoring activities, taking responsibility for 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

• Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
• Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection.
• Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
• Mentor and support junior CRAs, sharing knowledge and best practices.

Research Analyst jobs in France

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Senior Clinical Research Specialist

Senior Clinical Research Associate

Clinical Research Associate – Oncology

Clinical Research Associate II

Clinical Research Associate

Clinical Research Associate II – Sr Clinical Research Associate