
Senior Clinical Trial Coordinator
Há 24 horas
As a Central Monitoring Manager, you will be responsible for overseeing the development and execution of centralized monitoring plans across studies.
- Ensure consistency with RBQM strategy by reviewing and interpreting data quality trends and operational signals to identify emerging risks at the study, country, and site levels.
- Lead and manage a team of Central Monitors, providing guidance, oversight, and performance management.
- Contribute to risk assessments, periodic data reviews, and risk mitigation strategies in collaboration with cross-functional teams.
The ideal candidate will have a Bachelor's degree in a field relevant to clinical research and minimum 5 years of experience in centralized monitoring.
- 12+ years of clinical research experience across functions such as clinical monitoring, data management, biometrics, or project management.
- Experience in line management is a plus.
- Strong understanding of statistical monitoring principles, RBQM frameworks, and regulatory expectations related to clinical trial oversight.
Fluent English language skills are required, along with strong analytical and problem-solving abilities.
- Effective communication and interpersonal skills.
- Highly organized, with the ability to manage workload, timelines, and shifting priorities.
The successful candidate will possess knowledge of GCP, ICH guidelines, and applicable global regulations.
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