At a Glance
- Tasks: Lead data management for global clinical trials, focusing on oncology and neurology.
- Company: Innovative healthcare company dedicated to improving lives through science and technology.
- Benefits: Flexible working culture, personal development opportunities, and a diverse team.
- Other info: Join a culture of inclusion and innovation that empowers everyone.
- Why this job: Make a real impact in healthcare while working with cutting-edge technologies.
- Qualifications: 10+ years in clinical data management with leadership experience in complex trials.
The predicted salary is between 54000 - 66000 £ per year.
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! 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. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
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:
- As a senior team member within Clinical Data Management, you will lead the end-to-end data management delivery for assigned global Phase I–IV clinical trials or a defined study portfolio, with a particular focus on complex oncology, neurology or immunology development.
- You will set the strategic direction for data collection, cleaning, review, reconciliation, and quality activities, ensuring the accuracy, integrity, completeness, and submission-readiness of clinical trial data.
- Operating with a high degree of autonomy, you will serve as the primary Clinical Data Management representative at the study/program level, providing operational expertise and aligning cross-functional and global teams in a matrix organization.
- You will implement risk-based data management and data-flow strategies for in-house and outsourced studies, identify opportunities to apply automation, advanced analytics, and AI-enabled solutions to improve data quality and study execution, oversee CRO/vendor delivery, and support Health Authority submission activities by providing data management expertise and reviewing relevant materials.
- Beyond your study portfolio, you will actively shape the future of the function through process improvement initiatives, contributing to SOPs and best-practice workstreams, knowledge sharing, and mentoring colleagues to strengthen Clinical Data Management capability across the organization.
Who you are:
- You hold a Bachelor’s or Master’s degree in a scientific or technical discipline — life sciences, data management, or a related field.
- You have at least 10 years of experience in clinical data management within the pharmaceutical, biotechnology, or healthcare industry, including substantial leadership of complex oncology, neurology, or immunology trials at study and program level.
- You bring deep expertise in end-to-end data management, including risk-based data collection and cleaning strategies, eCRF design, external data management, and coding, with strong knowledge of CDISC, CDASH, and SDTM standards.
- You have a proven track record of managing CRO/vendor relationships, including operational performance oversight and budget monitoring, and are experienced in in-house sourcing models.
- You are skilled at leading and coordinating global, cross-functional teams in a matrix environment, and are confident providing updates on study progress, financials, forecasts, risks, issues, and timelines to senior stakeholders.
- You demonstrate strong project management capabilities — planning study timelines and resources, identifying and mitigating risks, resolving issues, and managing multiple priorities simultaneously with a high degree of independence.
- You are committed to continuous improvement and bring external insights to contribute to innovation, process development, and the evolution of data management standards and SOPs.
- Experience with Risk Based Data Monitoring and Management is preferred.
- Experience evaluating or implementing automation and/or AI-enabled innovations in clinical data management, with an understanding of data quality, traceability, validation, human oversight, and compliance considerations, is an advantage.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. 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!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
Associate Director Clinical Data Manager (all genders) in Taunton 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 Associate Director Clinical Data Manager (all genders) in Taunton
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Merck. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Merck.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Merck. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Merck is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Associate Director Clinical Data Manager (all genders) in Taunton
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Merck!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Merck that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Merck!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Merck, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Merck
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Merck that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Merck’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
