Clinical Study Manager

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.

We are seeking a Clinical Study Manager to lead the operational execution of our secondary data use Real World Evidence (RWE) activities and international clinical studies. In this role, you will coordinate end-to-end study operations across global sites, ensuring that our clinical programs deliver high-quality data safely, efficiently, and ethically. You will work within a highly collaborative, matrixed team environment where your leadership directly helps us bring medical innovations to patients faster.

• Lead Study Teams:
  Build and guide cross-functional, borderless study teams, establishing clear accountabilities, deliverables, and a psychologically safe environment where everyone can thrive
• Manage End-to-End Trial Operations:
  Maintain comprehensive study plans, risk mitigation strategies, site selection procedures and vendor oversight protocols from activation through to clinical closure
• Oversee Financials & Agreements:
  Manage study budgets, track metrics, review work orders and negotiate study agreements to ensure highly cost-effective operations with minimal variances
• Drive Global Regulatory Compliance:
  Ensure absolute adherence to international clinical trial guidelines such as Good Pharmacovigilance Practices and Good Pharmacoepidemiology Practices, relevant local regulations and inspection readiness
• Direct Vendor & Site Deliverables:
  Maintain strict oversight of external vendors, tracking performance metrics, resolving systematic operational issues and organising necessary training
• Develop Strategic Recruitment Plans:
  Analyze trial feasibility data across multiple countries to make data-driven recommendations on site distribution, patient numbers and retention strategies

You are a proactive, strategic operational leader with a passion for clinical excellence and cross-functional collaboration. You bring a growth mindset, excel at solving complex operational problems under tight deadlines, and possess deep listening and empathy skills that inspire your teams.

• Proven Clinical Leadership:
  Demonstrated experience leading successful study teams through all operational stages of clinical studies or secondary data use projects
• Regulatory Expertise: A clear understanding and practical experience applying global clinical quality requirements, regulations and pharmacovigilance standards
• Strategic Planning &
  
  Risk Management:
  
  Strong organisational awareness with a proactive planning mindset, including the ability to embed operational contingencies
• Financial & Vendor Acumen:
  Experience successfully managing trial budgets, processing vendor agreements and handling external system integrations
• Exceptional Communication:
  Well-developed written and verbal communication skills, with a proven ability to present clear directions, influence cross-functionally and resolve conflicts

Together, we’ll advance along the whole patient journey with the aspiration to prevent, stop and cure diseases. Join us in building a healthier future!

This position also offers an attractive benefits package. Learn more about how we reward our employees at Roche.

This job is posted in multiple locations. If you’re applying for the role in an alternative location where pay transparency regulations apply, the Talent Acquisition Partner will share the local pay information with you ahead of any business interview.

Roche is an Equal Opportunity Employer.