Clinical Data 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. The Data Manager (DM) plays a critical role in ensuring the quality, integrity, and availability of clinical trial data to support decision-making in early and late-stage drug development. Working closely with Biostatistics, Analytical Data Science, and cross-functional partners, the Data Manager leads the design, implementation, and oversight of data management activities across one or more studies. This includes database setup, data cleaning, query resolution, and vendor oversight, with a strong emphasis on regulatory compliance, efficiency, and data readiness for analysis. The role requires both technical acumen and collaborative leadership to anticipate challenges, drive process improvements, and enable high-quality data delivery across the clinical portfolio.

You support data management activities on clinical studies by generating and interpreting metrics related to CRF review, data entry check review, and query management under supervision
You apply foundational knowledge of clinical data systems and standards (e.g., CDISC) to ensure consistency and accuracy in data collection
You follow established procedures and use judgment to resolve routine data issues with moderate guidance
You understand study protocols, data flows, and team objectives to contribute effectively to assigned tasks
You communicate data issues clearly to internal team members and external vendors in straightforward situations
You apply independent judgment to solve moderately complex data issues, interpret guidance, prioritize responsibilities, and seek guidance in situations that require contextual understanding
You adhere to functional standards, participating in peer review or mentoring relationships to uphold quality while building expertise in data management methodology

You hold a Bachelor’s (or Master’s) degree in computer science, life sciences, statistics, informatics, or a related field
You have a minimum of 3-5 years of experience in clinical data management or a related function, or an advanced degree with 2+ years of equivalent work experience
You have a foundational understanding of clinical trial data and the drug development process
You are familiar with clinical data systems (e.g., EDC), Excel, and basic query logic
Internship or academic experience in clinical trials, data science, or informatics
SDTM) or basic programming (SAS, R)
Understanding of different data types (labs, eCOA, imaging)
Growth mindset with curiosity about how data drives drug development
Familiarity with common clinical data tools or platforms (e.g., Relocation benefits are not available for this job posting.

We use artificial intelligence to screen, assess or select applicants for this role.

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.

Roche is an Equal Opportunity Employer.