At a Glance
- Tasks: Lead global clinical trials, ensuring high-quality study designs and operational excellence.
- Company: Join Roche, a leader in healthcare innovation and patient care.
- Benefits: Competitive salary, inclusive culture, and opportunities for personal and professional growth.
- Other info: Dynamic, collaborative environment with a focus on advancing healthcare solutions.
- Why this job: Make a real impact on patient lives through innovative clinical research.
- Qualifications: Degree in Life Sciences and experience in clinical trial management required.
The predicted salary is between 60000 - 80000 £ per year.
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
At Roche Diagnostics Solutions (RDS), our mission is clear: to diagnose earlier, develop faster, and personalise treatment because every patient is unique. Our Clinical Development & Medical Affairs (CDMA) team drives innovation to improve healthcare outcomes globally. We see ourselves and our customers as a team that can only reach its full potential together. By listening closely to patients and physicians, and leveraging digitalisation and new technologies, we get closer to their real-world needs. This collaborative spirit creates an environment where ideas can grow and new ways of doing things can be tried - resulting in competitive products that get to patients faster.
Our work spans the entire product lifecycle, from discovery to post-launch. By collaborating with internal teams, external partners, and patients, the CDMA chapter provides crucial medical insights, designs and executes clinical studies, and offers on-market support. Ultimately, we generate the comprehensive clinical evidence that demonstrates product safety, effectiveness, and scientific validity - facilitating smooth product registration, adoption and reimbursement globally so we can save lives and improve patient quality of life.
The Opportunity
As a Global Study Lead, you will take full accountability for the design, planning, and execution of global sponsored clinical trials from protocol development through to close-out. Joining a dynamic, matrixed team within our Clinical Development and Medical Affairs communities, you will oversee diverse study portfolios, including companion diagnostics, early adopter programs, and research collaborations, ensuring operational excellence, budget control, and absolute inspection readiness.
- Drive Study Excellence: Lead the global cross-functional study team with full accountability for high-quality study designs, clinical deliverables, budgets, and timelines.
- Shape Evidence Strategies: Partner with Program Leadership to map out innovative scenarios for global evidence generation, collaborating across Regulatory Affairs, R&D, and medical project teams.
- Author Core Study Documentation: Develop critical, high-impact clinical documents including study protocols, Design Validation Plans, study forms, and comprehensive study reports.
- Champion Strategic Partnerships: Oversee external service providers and Contract Research Organisations (CROs), driving vendor performance, selection, and relationship management at the study level.
- Advance Diagnostics Innovation: Direct the operational aspects of companion diagnostics studies sponsored by external partners alongside early access and research collaboration portfolios.
- Cultivate Expert Networks: Collaborate closely with international medical opinion leaders, investigators, and key external stakeholders to bring advanced external insights in-house.
Who You Are
You are a proactive, analytical clinical operations professional who thrives in fast-paced, global environments. You bring a collaborative mindset, excellent communication skills, and a passion for delivering life-changing clinical insights.
- A degree in Life Sciences, Healthcare, or a related scientific field (an advanced degree is a plus).
- Strong, progressive experience in clinical trial management or study-level execution within the healthcare, pharmaceutical, or biotechnology sectors. Preferably experience study managing Molecular IVD clinical trials.
- Solid working knowledge of clinical research standards and global regulations (such as ICH-GCP, IVDD/IVDR, MDR, SaMD, or FDA frameworks).
- Demonstrated ability to manage external suppliers (like CROs) and successfully manage complex project budgets.
- Exceptional verbal and written communication skills in English, with a proven ability to lead project substreams, build consensus, and work fluidly across diverse regions and cultures.
Together, we’ll advance along the whole patient journey with the aspiration to prevent, stop and cure diseases. Apply today to help us shape the future of clinical operations!
Global Study Lead (Molecular Lab) in Motherwell employer: F. Hoffmann-La Roche AG
At Roche, we pride ourselves on fostering a culture that values personal expression and open dialogue, making it an exceptional place to work as a Global Study Lead. Our commitment to innovation in healthcare is matched by our dedication to employee growth, offering opportunities for professional development within a collaborative and dynamic environment. With locations like Burgess Hill and Vienna, employees benefit from a vibrant work culture that encourages teamwork and creativity, all while contributing to meaningful advancements in patient care.
StudySmarter Expert Advice🤫
We think this is how you could land Global Study Lead (Molecular Lab) in Motherwell
✨Tip Number 1
Network like a pro! Reach out to people in your field on LinkedIn or at industry events. A friendly chat can lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their mission and values, so you can show how you fit right in with their team.
✨Tip Number 3
Practice your pitch! Be ready to explain your experience and how it relates to the role. Keep it concise but impactful – you want to leave them wanting to know more about you.
✨Tip Number 4
Don’t forget to follow up after interviews! A quick thank-you email can keep you top of mind and shows your enthusiasm for the position. Plus, it’s just good manners!
We think you need these skills to ace Global Study Lead (Molecular Lab) in Motherwell
Some tips for your application 🫡
Show Your Passion:When writing your application, let your enthusiasm for the role shine through! We want to see how your passion for clinical trials and healthcare aligns with our mission at Roche.
Tailor Your CV:Make sure to customise your CV to highlight relevant experience in clinical trial management. We love seeing how your background fits with the Global Study Lead position, so don’t hold back!
Be Clear and Concise:Keep your application straightforward and to the point. We appreciate clarity, so make sure your skills and experiences are easy to spot. Use bullet points if it helps!
Apply Through Our Website:Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. We can’t wait to hear from you!
How to prepare for a job interview at F. Hoffmann-La Roche AG
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trial management and the specific regulations like ICH-GCP and IVDR. Being able to discuss these topics confidently will show that you're not just familiar with the basics, but that you truly understand the complexities involved in global studies.
✨Show Your Collaborative Spirit
Since this role involves working with diverse teams and external partners, be ready to share examples of how you've successfully collaborated in the past. Highlight your communication skills and how you've built consensus across different stakeholders to drive projects forward.
✨Prepare for Scenario Questions
Expect questions that ask you to think on your feet about potential challenges in study design or execution. Prepare some scenarios where you had to problem-solve or innovate under pressure, especially in a fast-paced environment. This will demonstrate your analytical skills and proactive mindset.
✨Ask Insightful Questions
At the end of the interview, don’t shy away from asking questions that show your interest in the company’s mission and culture. Inquire about their approach to innovation in diagnostics or how they foster collaboration within teams. This not only shows your enthusiasm but also helps you gauge if the company is the right fit for you.
