At a Glance
- Tasks: Lead data management for global clinical trials and ensure submission-ready data.
- Company: Join a diverse and inclusive healthcare company focused on innovation.
- Benefits: Flexible working, personal development opportunities, and a culture of belonging.
- Other info: Collaborate with global teams and promote automation in data management.
- Why this job: Make a real impact in healthcare by shaping data practices globally.
- Qualifications: 8+ years in clinical data management with strong project management skills.
The predicted salary is between 54000 - 66000 £ per year.
Overview
In this role you will own the delivery, quality, and submission-readiness of clinical trial data for global Phase I–IV studies.
You’ll implement risk-based data collection and QA across EDC and external sources, represent Data Management on the Core Trial Team, and lead study-level data deliverables and timelines.
You’ll oversee CRO/vendor activities, ensure regulatory alignment, and drive data management standardization and automation initiatives.
This position offers cross-functional collaboration across a global team and opportunities to shape data practices in healthcare trials.
- Pay / Benefits
- diverse and inclusive culture
- flexible working environment
- opportunities for personal and career development
- global collaboration and impact
- culture of inclusion and belonging
- focus on innovation in science and technology
Responsibilities
- Deliver end-to-end data management for global clinical trials (Phase I–IV)
- Implement risk-based data collection, cleaning, reconciliation, and QA across EDC and external data sources
- Represent Clinical Data Management on the Core Trial Team
- Lead study-level data management deliverables, including timelines and resources
- Coordinate CRO/vendor activities and manage operational issues
- Ensure regulatory compliance and submission-ready data packages
- Support adherence to CDISC standards and regulatory requirements
- Contribute to evolution of data management standards, SOPs, and process improvements; promote automation/AI where appropriate
- Mentor colleagues and share knowledge within Clinical Data Management
- Key requirements
- Bachelor’s or Master’s degree in life sciences, data management, or related field
- ≥8 years of clinical data management experience in pharma/biotech/healthcare
- Proven track record of end-to-end data management for global trials
- Strong project management, communication, collaboration, and problem-solving skills
- Experience coordinating global cross-functional teams and CRO/vendor activities
- Proficiency with clinical data management systems and tools
- Good understanding of regulatory requirements and CDISC data standards
- Commitment to continuous development and knowledge sharing in data management
- Experience with Risk Based Data Monitoring preferred
- Experience with automation, advanced analytics, and AI-enabled solutions is an advantage
- strong communication
- collaboration
- problem-solving
- clinical data management systems and tools
- CDISC standards
- regulatory knowledge and submission-ready data packages
Senior Clinical Data Manager (all genders) in Feltham employer: Merck
Join a dynamic team in Livingston where innovation meets inclusivity! As a Production Operator in our cleanroom, you'll benefit from a supportive work culture that values diverse perspectives and fosters personal growth. With opportunities for professional development and a commitment to employee well-being, we empower you to make a meaningful impact in the fields of Healthcare, Life Science, and Electronics.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Clinical Data Manager (all genders) in Feltham
✨Get Involved with Local Health Initiatives
Join local community health events or volunteer for organisations like public health agencies. This not only builds your experience but also helps you network with industry professionals who might know of openings at places like Merck.
✨Tap into Professional Associations
Check out associations like the Institute of Healthcare Management. They often have job boards, networking events, and conferences that are perfect for connecting with potential employers in health sciences administration.
✨Stay Updated with Industry Trends
Follow health policy news and trends—being knowledgeable about the current landscape will not only help you in interviews but also make you stand out as a candidate. You can discuss recent developments and their implications when chatting with folks at Merck.
✨Apply Through Our Website for Better Visibility
When you find roles that excite you, especially at places like Merck, don’t forget to apply through our website. This can sometimes give you an edge by showing the employer you’re savvy and committed to finding the right fit.
We think you need these skills to ace Senior Clinical Data Manager (all genders) in Feltham
Some tips for your application 🫡
Highlight Your Relevant Experience:When applying for a role in health sciences administration, it's super important to spotlight any relevant experience you have in healthcare settings. Whether you've worked in a hospital, a clinic, or any related environment, make sure to detail those roles in your CV – focusing on your responsibilities and achievements that align with the job at Merck.
Showcase Your Administrative Skills:Administrative skills are key in this field, so don’t hold back! Make sure your CV reflects your proficiency in things like scheduling, data management, and compliance with health regulations. Mention specific software you’ve used, such as patient management systems, as this will demonstrate your hands-on abilities and readiness for the role at Merck.
Craft a Meaningful Cover Letter:Your cover letter should reflect your passion for the health sciences field and your eagerness to contribute to Merck. Share a bit about why you’re drawn to this sector, any impactful situations or challenges you’ve encountered, and how they’ve shaped your desire to work in health sciences administration. This personal touch can really set you apart!
Tailor Your Documents to the Job:Don't use a one-size-fits-all approach! Make sure your CV and cover letter are specifically tailored for this role. Highlight any certifications you have relevant to health administration, and ensure you clearly connect your previous roles to the skills needed for the full-time position at Merck. This way, you're showing them you’ve done your homework and are genuinely interested in being a part of their team.
How to prepare for a job interview at Merck
✨Showcase Your Administrative Skills
In health sciences administration, being organised is key. Make sure you can demonstrate your skills in managing schedules, paperwork, and data accurately. Be ready to discuss specific tools you've used, like electronic health record systems or scheduling software, and how they improved efficiency in your past experiences.
✨Know Your Regulations
Familiarity with healthcare regulations and compliance is crucial. Brush up on HIPAA, GDPR, or other relevant policies before your interview. We recommend preparing examples of how you've ensured compliance or handled sensitive information in past roles—this will show you're not just knowledgeable but also responsible.
✨Prepare for Scenario Questions
Interviews for administrative roles often involve scenario-based questions to assess your problem-solving skills. Practice responses to common situations you might face, such as dealing with a challenging patient or managing a sudden schedule change. This will not only demonstrate your ability to think on your feet but also highlight your interpersonal skills.
✨Align Your Goals with the Organisation
As a full-time candidate, employers will want to know how your long-term career goals align with their mission. Take some time to research Merck’s values and be ready to tie your passion for health sciences administration into their objectives. Demonstrating enthusiasm and career alignment can be a game-changer in this competitive field!
