At a Glance
- Tasks: Lead clinical data management for global studies and ensure data quality and integrity.
- Company: Innovative healthcare company focused on improving lives through science and technology.
- Benefits: Attractive salary, comprehensive health coverage, generous PTO, and career development opportunities.
- Other info: Join a culture of inclusion and innovation that empowers personal and professional growth.
- Why this job: Make a real impact in healthcare while working with cutting-edge technologies and diverse teams.
- Qualifications: 8+ years in clinical data management with strong project management and communication skills.
The predicted salary is between 59400 - 72600 £ per year.
Work Your Magic with us! Ready to explore, break barriers, and discover more? Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
This role requires to be on-site in our office in Feltham for 3 days per week.
Your role:
- 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 electronic data capture (EDC) and external data sources.
- You will lead the project management of all study-level data management deliverables, including timeline planning, resource coordination, risk identification, issue resolution, and stakeholder communication across internal and external partners.
- You will oversee day-to-day CRO/vendor activities, support compliance with regulatory requirements and industry standards such as CDISC, and help ensure that clinical data packages are complete, accurate, and submission ready.
- You will contribute to the evolution of data management standards, SOPs, best practices, and process improvements, including the effective use of automation, advanced analytics, and AI-enabled solutions where appropriate.
- You will share knowledge and support the development of colleagues within Clinical Data Management.
Who you are:
- You hold a Bachelor's or Master's degree in a scientific or technical discipline, preferably in life sciences, data management, or a related field.
- You have a minimum of 8 years of experience in clinical data management within the pharmaceutical, biotechnology, or healthcare industry.
- You bring strong project management, communication, collaboration, and problem-solving skills.
- You have experience coordinating global, cross-functional teams in a matrix organization.
- You are proficient in clinical data management systems and tools, with sound knowledge of regulatory requirements, industry standards, and good practices in clinical data management.
- You have experience with clinical trial data standards, including CDISC.
- You are committed to continuous personal and professional development.
- Experience with Risk Based Data Monitoring and Management is preferred.
- Experience using or supporting the implementation of automation, advanced analytics, and/or AI-enabled solutions in clinical data management is an advantage.
What we offer:
- We offer a range of attractive benefits to help you work your magic.
- We are committed to creating access and opportunities for all to develop and grow at your own pace.
- Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Senior Clinical Data Manager employer: Merck Group
Join a forward-thinking healthcare company in Feltham, UK, where innovation meets compassion. As a Clinical Site Management Excellence Lead, you'll thrive in a diverse and inclusive culture that prioritises personal development and career advancement. With a commitment to excellence in clinical research and a focus on improving lives globally, this role offers the unique opportunity to shape the future of healthcare while working alongside passionate colleagues dedicated to making a difference.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Clinical Data Manager
✨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 Group.
✨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 Group.
✨Apply Through Our Website for Better Visibility
When you find roles that excite you, especially at places like Merck Group, 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
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 Group.
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 Group.
Craft a Meaningful Cover Letter:Your cover letter should reflect your passion for the health sciences field and your eagerness to contribute to Merck Group. 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 Group. 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 Group
✨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 Group’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!
