Senior Clinical Data Manager

Merck Group; London Borough of Hounslow; On-site; GBP 90,000 - 120,000; Full time

Job summary

Merck Group in Feltham is seeking a Senior Clinical Data Manager to ensure delivery, quality, integrity, and submission-readiness of clinical trial data for 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.

This role leads day-to-day CRO/vendor activities, ensuring compliance with regulatory requirements and

Qualifications

• Bachelor's or Master's degree in a scientific or technical discipline, preferably life sciences or data management.
• 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.

Responsibilities

• Delivery, quality, integrity, and submission-readiness of clinical trial data for global Phase I-IV studies.
• Lead project management of study-level data management deliverables and oversee CRO/vendor activities, supporting compliance with regulatory requirements and standards such as CDISC.
• Represent Clinical Data Management on the Core Trial Team.

Skills

Project management

Cross-functional coordination

Communication skills

Problem solving

CRO/vendor coordination

Regulatory knowledge

CDISC familiarity

Education

Bachelor's or Master's in life sciences or data management

Job description

Work Your Magic with us!

Ready to explore, break barriers, and discover more? Our colleagues across the globe innovate with science and technology to enrich people's lives across Healthcare, Life Science, and Electronics.

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.