At a Glance
- Tasks: Lead global clinical trials and collaborate with cross-functional teams to drive innovation.
- Company: Join Roche Diagnostics, a leader in healthcare and diagnostics.
- Benefits: Flexible working options, competitive salary, and opportunities for professional growth.
- Other info: Dynamic role with international collaboration and career advancement opportunities.
- Why this job: Make a real impact in healthcare by managing cutting-edge clinical studies.
- Qualifications: Degree in Life Sciences or related field; experience in clinical trial management preferred.
The predicted salary is between 60000 - 80000 £ per year.
Position Global Study Lead within Roche Diagnostics Solutions (RDS) Clinical Development & Medical Affairs (CDMA) team, responsible for design, planning, and execution of global sponsored clinical trials.
Responsibilities
- Lead global cross‑functional study team with full accountability for study designs, clinical deliverables, budgets, and timelines.
- Collaborate with Program Leadership to map innovative global evidence scenarios, coordinating with Regulatory Affairs, R&D and medical project teams.
- Develop clinical documents including study protocols, Design Validation Plans, study forms, and comprehensive study reports.
- Oversee external service providers and CROs, driving vendor performance, selection, and relationship management at the study level.
- Direct operational aspects of companion diagnostics studies and early access / research collaboration portfolios.
- Collaborate with international medical opinion leaders, investigators and key external stakeholders to incorporate external insights.
- Ensure operational excellence, budget control, and inspection readiness across diverse study portfolios.
Qualifications
- Degree in Life Sciences, Healthcare, or related scientific field (advanced degree is a plus).
- Strong, progressive experience in clinical trial management or study-level execution within healthcare, pharmaceutical or biotechnology sectors.
- Preferably experience managing molecular IVD clinical trials.
- Solid knowledge of clinical research standards and global regulations (ICH‑GCP, IVDD/IVDR, MDR, SaMD, or FDA frameworks).
- Demonstrated ability to manage external suppliers, including CROs, and successfully manage complex project budgets.
- Exceptional verbal and written communication skills in English, with proven ability to lead project substreams, build consensus, and work fluidly across diverse regions and cultures.
Location
Primary location: Burgess Hill. Additional locations may be discussed during the hiring process.
EEO Statement
All qualified applicants will receive consideration for employment without regard to race, religion, belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability, or age. We recognize the importance of flexible working and will review all applicants’ requests with care.
Global Study Lead (Molecular Lab) employer: F. Hoffmann-La Roche AG
Roche Diagnostics Solutions is an exceptional employer that fosters a collaborative and innovative work culture, particularly for the Global Study Lead role in Burgess Hill. Employees benefit from comprehensive professional development opportunities, flexible working arrangements, and the chance to engage with leading experts in the field, all while contributing to impactful clinical trials that advance healthcare solutions globally.
StudySmarter Expert Advice🤫
We think this is how you could land Global Study Lead (Molecular Lab)
✨Tip Number 1
Network like a pro! Reach out to your connections in the healthcare and clinical trial sectors. Attend industry events or webinars where you can meet potential colleagues or mentors who might help you land that Global Study Lead role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH-GCP and other relevant regulations. We want you to showcase your expertise in clinical trial management, so be ready to discuss your experience managing complex projects and budgets.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a thank-you email to express your appreciation and reiterate your interest in the position. It shows professionalism and keeps you fresh in their minds.
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at Roche Diagnostics Solutions.
We think you need these skills to ace Global Study Lead (Molecular Lab)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that align with the Global Study Lead role. Highlight your clinical trial management experience and any relevant qualifications in Life Sciences or Healthcare.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about this role at Roche Diagnostics Solutions and how your background makes you the perfect fit for leading global clinical trials.
Showcase Your Communication Skills:Since exceptional communication is key for this position, ensure your written application is clear, concise, and free of jargon. This will demonstrate your ability to convey complex information effectively.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets the attention it deserves and allows us to keep track of all applicants efficiently.
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 FDA frameworks. Being able to discuss these confidently will show that you're not just familiar with the basics, but that you really understand the complexities involved in global studies.
✨Showcase Your Experience
Prepare to share specific examples from your past roles where you've successfully managed clinical trials or collaborated with cross-functional teams. Highlight any experience with molecular IVD clinical trials, as this will be particularly relevant for the role.
✨Communicate Clearly
Since exceptional communication skills are a must, practice articulating your thoughts clearly and concisely. You might want to rehearse answers to common interview questions, focusing on how you can lead project substreams and build consensus among diverse teams.
✨Ask Insightful Questions
Prepare some thoughtful questions about the company's approach to clinical trials and how they collaborate with external stakeholders. This shows your genuine interest in the role and helps you gauge if the company culture aligns with your values.
