At a Glance
- Tasks: Lead global study teams and ensure high-quality study designs for impactful research.
- Company: Join a leading pharmaceutical company dedicated to innovation and patient care.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with strong focus on operational excellence and career advancement.
- Why this job: Make a real difference in healthcare by managing cutting-edge studies.
- Qualifications: Bachelor's degree in Life Sciences and 5+ years of relevant experience required.
The predicted salary is between 60000 - 80000 € per year.
Responsibilities
- Leads the global study team with full accountability for the study deliverables with respect to quality, budget and timelines, in collaboration with the Study Team.
- Ensures the development of high quality study designs for sponsored studies in collaboration with internal and external experts.
- In collaboration with Program Leadership, prepares different scenarios for evidence generation (e.g. study, real-world evidence) in cross-functional collaboration (e.g. with Regulatory Affairs, R&D, CDMA Project Teams) to support global strategies and planning of timeline and costs.
- Develops key study documents (i.e., Design Validation Plan, protocol, study training materials, study forms and templates, study report).
- Oversees planning and operational aspects of companion diagnostics studies sponsored by Pharma partners.
- Accountable for study-level budget of assigned studies.
- Adherence to regulations, guidelines and standard operating procedures, and ensures audit/inspection readiness.
- Execution of sponsored studies for assigned areas of focus for registrational and/or non-registrational purposes through all study phases (planning, start-up, conduct and close-out).
- Oversees study activities outsourced to a service provider (i.e., CRO).
- Ensure that study results are published in collaboration with the Publication Team.
- Oversees projects to ensure completion on-time, within scope and budget; and tracks project performance to analyze the completion of short and long term goals.
- Build and maintain strong, collaborative relationships with cross-functional leaders, key internal and external stakeholders and other alliance partners, including CROs, in meeting business goals and ensuring operational excellence.
Qualifications
- You have a bachelor's degree in Life Sciences or related field.
- You have 5+ years of experience managing the full lifecycle of sponsored studies, ensuring projects meet performance goals within scope, quality, budget, and timeline.
- You have extensive experience in ensuring that study results are published in collaboration with the Publication Team.
- You have in-depth knowledge and experience in the role of Clinical Operations in product development; are aware of Roche's place in the market and our value proposition to patients and customers.
- You have experience with PHCS and Companion Diagnostic trials, specifically within pathology and core lab indications.
- You have experience managing complex projects by using analytical judgment and innovative thinking to assess risks and solve difficult problems.
- You have prior experience building and maintaining strong, collaborative relationships with cross-functional leaders, key internal and external stakeholders and other alliance partners, including Pharma partners or CROs, in meeting business goals and ensuring operational excellence.
Preferred Qualifications
- You have an advanced degree in Life Sciences or a related field.
Global Study Lead in City of Westminster employer: Roche
Roche is an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of life sciences. With a strong commitment to employee growth, Roche provides numerous opportunities for professional development and advancement, ensuring that team members are equipped to lead impactful global studies. Located in a vibrant environment, employees benefit from a supportive atmosphere that values diversity and inclusion, making it a truly rewarding place to work.
StudySmarter Expert Advice🤫
We think this is how you could land Global Study Lead in City of Westminster
✨Network Like a Pro
Get out there and connect with people in the industry! Attend events, join online forums, and don’t be shy about reaching out to professionals on LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Ace the Interview
Prepare for your interviews by researching the company and the role inside out. Practice common interview questions and think about how your experience aligns with the responsibilities of a Global Study Lead. We want you to walk in feeling confident and ready to impress!
✨Showcase Your Skills
When you get the chance to present your work or discuss your projects, make sure to highlight your achievements and how they relate to the job. Use specific examples that demonstrate your ability to manage studies and collaborate with teams. We love seeing candidates who can back up their claims with real-life success stories!
✨Apply Through Our Website
Don’t forget to apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we’re always on the lookout for passionate individuals who are ready to take on exciting challenges in the world of clinical operations.
We think you need these skills to ace Global Study Lead in City of Westminster
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the Global Study Lead role. Highlight your experience in managing sponsored studies and any relevant projects you've led, as this will show us you're a great fit!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about the role and how your background aligns with our needs. Don't forget to mention your experience with cross-functional collaboration and project management.
Showcase Your Achievements:When detailing your past roles, focus on specific achievements that demonstrate your ability to meet performance goals within scope, quality, budget, and timeline. We love seeing quantifiable results that highlight your impact!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re keen on joining the StudySmarter team!
How to prepare for a job interview at Roche
✨Know Your Stuff
Make sure you’re well-versed in the specifics of global study management and the lifecycle of sponsored studies. Brush up on your knowledge of clinical operations, especially regarding PHCS and Companion Diagnostic trials. This will help you answer questions confidently and show that you’re the right fit for the role.
✨Showcase Your Experience
Prepare to discuss your past experiences managing complex projects. Use specific examples that highlight your ability to meet performance goals within scope, quality, budget, and timeline. This will demonstrate your capability to handle the responsibilities outlined in the job description.
✨Build Relationships
Since the role involves collaboration with various stakeholders, be ready to talk about how you’ve built and maintained strong relationships in previous roles. Share examples of how you’ve worked with cross-functional teams and external partners to achieve common goals.
✨Be Audit-Ready
Familiarise yourself with regulations, guidelines, and standard operating procedures relevant to clinical studies. Being able to discuss how you ensure audit and inspection readiness will show that you take compliance seriously, which is crucial for this position.
