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This role requires you to be on-site in our Feltham office for 3 days per week.
Your role
As a Senior Clinical Data Manager, you will be accountable for the delivery, quality, integrity, and submission-readiness of clinical trial data for assigned global Phase I-IV studies. You will implement risk-based data collection, cleaning, review, reconciliation, and quality activities across EDC and external data sources, and represent Clinical Data Management on the Core Trial Team. You will lead project management of study-level data management deliverables and oversee day-to-day CRO/vendor activities, supporting compliance with regulatory requirements and standards such as CDISC.
Who you are
- A Bachelor’s or Master’s degree in a scientific or technical discipline, preferably life sciences or data management
- A minimum of 8 years of clinical data management experience in pharmaceutical, biotechnology, or healthcare, including end-to-end delivery for global trials
- Strong project management, communication, collaboration, and problem-solving skills
- Experience coordinating global, cross-functional matrix teams and managing CRO/vendor activities
- Proficiency in clinical data management systems and knowledge of regulatory requirements and good practice
- Experience with clinical data standards including CDISC
Preferred:
Risk Based Data Monitoring and Management experience, and experience with automation, advanced analytics, or AI-enabled solutions in clinical data management.
Merck Group is committed to creating access and opportunities for all to develop and grow at their own pace.
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