Data Manager
About the role
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
Not included in the source posting: benefits.
Skills
Who can apply
The employer didn't state any visa, work authorization, citizenship or clearance requirements in this posting. Confirm with the employer before applying.
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