Clinical Research Scientist

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.

The Position

The Roche Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late stage development (Phase 2-3) clinical strategies and plans to deliver medically-differentiated therapies that provide meaningful improvement to patients.

The Opportunity

Join Roche/Genentech as a Lead/Senior Clinical Scientist and play a pivotal role in advancing the clinical development of Prasinezumab,  the first anti-synuclein antibody entering Phase III development and with the potential to be the first disease modifying treatment for Parkinson’s disease. This position offers a unique opportunity to contribute to ground-breaking drug development in Neurology, collaborate with cross-functional global teams, and drive progress in Parkinson’s clinical development. 

• Collaborate with cross-functional teams to design, implement, monitor, and analyze clinical studies.
• Develop and maintain key clinical documents, including study protocols, investigator brochures, informed consent forms, and progress reports.
• Provide oversight of and contribute to Medical Data Review Plan execution
• Make significant contributions to clinical development planning
• Contribute to clinical science strategy for various activities, including regulatory interactions
• Stay abreast of relevant scientific literature and integrate findings into clinical strategy planning.
• Review, interpret, and present clinical trial data internally and externally.
• Ensure adherence to GCP, regulatory standards, and quality protocols.
• Work closely with global teams through frequent collaboration.

Who You Are

You’re a highly motivated professional passionate about influencing your own development and making an impact in Neurology. You bring:

• An advanced degree (PhD or PharmD preferred) and 3-5 years of drug development experience within the biopharmaceutical industry.
• Demonstrated expertise in clinical trials, with a focus on Phase II or III trials including authoring of protocols and/or protocol amendments .Experience in neurodegeneration and/or in early stage development and processes is a plus
• Interested in and motivated by study execution related activities, incl. data review
• Strong ability to interpret and synthesize scientific data and present it effectively in diverse settings.
• Excellent written and verbal communication skills.
• A collaborative mindset, thriving as a team player in a global matrix environment.

Are you ready to help shape the future of Parkinson’s disease treatment? Join us and make your mark.

Who We Are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.