Senior Clinical Research Associate
Posted 7 hours ago
Posted 7 hours ago
This is a fully remote position, open to applicants in France.
• Overseeing clinical trial sites to guarantee compliance with study protocols, regulatory standards, and Good Clinical Practice (GCP) guidelines.
• Performing site visits to evaluate site performance, troubleshoot issues, and provide assistance to ensure successful execution of trials.
• Collaborating with multidisciplinary teams to ensure timely and precise data collection and reporting.
• Offering training and support to site personnel and other Clinical Research Associates (CRAs) to uphold high standards of clinical trial conduct.
• Establishing and nurturing effective relationships with site staff and stakeholders to promote seamless trial operations.
• Advanced degree in a relevant discipline such as life sciences, nursing, or medicine.
• Significant experience as a Clinical Research Associate, with a solid understanding of clinical trial processes and regulatory frameworks.
• Demonstrated ability to manage multiple sites and projects concurrently, with strong organizational and problem-solving capabilities.
• Proficiency in monitoring practices, data integrity, and site management, along with experience using relevant clinical trial software and tools.
• Exceptional communication, interpersonal, and stakeholder management abilities, with the capacity to influence and ensure compliance within a complex environment.
• Willingness to travel at least 60% of the time (both internationally and domestically - via flying and driving) and possess a valid driver’s license.
• Competitive base salary along with performance-related incentives.
• Health and wellness programs, including medical, dental, and vision coverage where applicable.
• Retirement and pension schemes.
• Life insurance and disability coverage.
• Employee assistance programs and wellness resources.
• Opportunities for learning and development through structured training and career advancement pathways.
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