Hiring.Camp

Data Manager

Roche

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Location
Welwyn, United Kingdom
Type
Full-time
Seniority
Manager
Experience
2+ years
Closing date
Today
Source
Workday

Description

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

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. 

This role is based in Data Management, a core function within Product Development Data Sciences (PDD). We lead the industry in speed and efficiency across all data management responsibilities. We achieve this through the development of tools, automation, and the adoption of cutting-edge technologies that streamline clinical trial data collection and delivery. 

As trusted partners in end-to-end drug development, Data Management leverages deep expertise in cross-therapeutic area data modalities to lead and influence clinical trial data strategy across Roche. We balance the need for high-quality outputs with fit-for-purpose data collection, enabling faster, more efficient trials that support timely decision-making and accelerate the delivery of new medicines to patients. 


The Opportunity: 


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 share learnings and emerging best practices with peers to support team development
  • 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 

Who you are: 

  • 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 2-4 years of experience in clinical data management or a related function, or an advanced degree with 0-2 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
  • You demonstrate strong attention to detail and organizational skills 
  • You demonstrate critical thinking and a willingness to learn 
  • You are an effective communicator, able to work collaboratively in team settings
  • You demonstrate respect for cultural differences when interacting with colleagues in the global workplace 

Preferred: 

  • Internship or academic experience in clinical trials, data science, or informatics
  • Exposure to CDISC standards (e.g., 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., Medidata RAVE) 

Location 

  • This position is based in Welwyn
  • Relocation Assistance is not available 

 

 

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.

Skills

Data ScienceExcelClinical TrialsComplianceR

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