Senior Clinical Project Scientist (m/f/d)

VIATRIS INNOVATION GMBH

Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases.

We have been included on number of that demonstrate the impact we are making.

Our Story

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We do so:

• Access– Providing high quality trusted medicines regardless of geography orcircumstance;

• Leadership– Advancing sustainable operations and innovative solutions to improve patient health; and

• Partnership– Leveraging our collectiveexpertiseto connect people to products and services.

Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education,outreachand better access to treatment.

For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world.

As a Senior Clinical Project Scientist, you play a key scientific role within cross-functional clinical trial teams and work closely with the Clinical Project Physician to drive high-quality clinical development programs.

Key responsibilities:

• Act as a scientific partner to the Clinical Project Physician across clinical programs
• Lead or contribute to the authoring of core trial documents such as protocols, ICFs, IBs, CSRs, and development plans
• Provide scientific input into medical monitoring, data review, and trial oversight
• Engage with external clinical experts and organize expert meetings
• Contribute to regulatory interactions (e.g. End-of-Phase II, SAWP/CHMP, pre‑NDA)
• Support lifecycle management activities from early development to post‑approval
• (Senior/Expert level) Contribute to clinical leadership, mentoring, and business development / due diligence activities

Your profile:

• Advanced degree in life or health sciences (PhD, PharmD, MSc or equivalent)
• Extensive experience in a pharmaceutical company or CRO, with strong exposure to Phase II–III clinical trials
• Proven experience authoring and reviewing scientific and clinical trial documents
• Solid understanding of clinical trial design, statistics, regulatory requirements, and drug development processes
• Confidence in working within global, cross-functional teams
• Fluent English (written and spoken)
• Structured, proactive, and results-oriented working style

Why Viatris:
Make a real global impact on patient access to medicines

• Work in an international, science-driven environment
• High level of scientific ownership and visibility
• Collaborative culture with room to grow, lead, and influence
• Attractive compensation and benefits, aligned with your experience
• Hybrid working opportunity (3 days onsite/2days remote)

At Viatris, we offercompetitivesalaries, benefitsandan inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer.