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

This Associate Evidence Manager role is seated in the Clinical Validation subchapter within the Digital Technology Health Information (DTHI) function for Roche Information Solutions (RIS), where it drives evidence-generation activities for assigned digital health solutions. It requires an individual with experience of clinical research and sound understanding of digital health solutions, who thrives in a fast-paced, agile environment and brings a proactive, growth-oriented mindset.

The Opportunity:

• Manage the process of evidence planning for assigned digital health solutions, incl. documenting integrated evidence plan.

• Ensure contracting with research collaborators is fast, compliant and provides a good experience for external collaborators.

• Develop study protocols and ensure that they are reviewed by relevant internal and external stakeholders to meet internal processes and timelines.

• With guidance of evidence leads, ensure that approved studies are managed to internal standards, timelines and budgets.

• With guidance of evidence leads, create and provide metrics on upcoming and ongoing studies.

• WIth guidance of evidence leads, ensure follow up on contractual deliverables from both Roche and Investigator side, e.g. implementation of digital tools, provision of manuscripts etc.

• With guidance of evidence leads, ensure team members (e.g. evidence team, data scientists etc..) conduct timely data analysis of study results, and develop and delivery evidence outputs

• Support evidence leads to provide regular evidence status reports in line with the evidence plan.

• Ensure work with collaborators is knowledgeable, responsive and provides a good experience for stakeholders.

Who You Are

• Master degree (or above) in a life science discipline and PhD/MD degree preferred

• Previous experience in medical & scientific affairs in industry or academic setting

• Good project management skills

• Good understanding of research methodologies

• Knowledge of clinical operations and/or clinical data management in Industry (Pharma/Diagnostics)

• Knowledge of the evaluation of digital health solutions

• Good understanding of research methodologies and data analysis

• Good scientific communication (writing & presenting)

• Fluency in English

This position is based in Rotkreuz. At the Company's discretion, an exception to the location requirement could be made under extraordinary circumstances.  

As this position is a global role, international business travel will be required depending upon the business location of the successful candidate and ongoing business project activities.

Please note that a preferred candidate has been identified for this position

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.

Roche is an Equal Opportunity Employer.