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? 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, and 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!
Associate Director Clinical Data Manager (all genders) employer: Merck Healthcare
At our Feltham office, we pride ourselves on being an exceptional employer that fosters a diverse and inclusive work culture, where innovation thrives and personal development is encouraged. As part of our Healthcare team, you will have the opportunity to lead impactful clinical data management projects while collaborating with passionate colleagues across the globe, all within a flexible environment that supports your career advancement and well-being.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director Clinical Data Manager (all genders)
✨Get Involved with Local Health Initiatives
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We think you need these skills to ace Associate Director Clinical Data Manager (all genders)
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 Healthcare.
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 Healthcare.
Craft a Meaningful Cover Letter:Your cover letter should reflect your passion for the health sciences field and your eagerness to contribute to Merck Healthcare. 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 Healthcare. 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 Healthcare
✨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 Healthcare’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!