Data Manager - Clinical Trials

About the Role

Our client is looking for a highly skilled Data Manager to join their clinical operations team, based in Norwich, Norfolk, UK . In this vital role, you will be responsible for the design, development, and management of clinical trial databases, ensuring the integrity, accuracy, and quality of data collected across multiple studies. You will work closely with clinical operations, biostatistics, and programming teams to define data management standards and processes. This position is crucial for enabling robust data analysis and supporting regulatory submissions. The role offers a dynamic environment with a hybrid working model, combining office-based collaboration with remote flexibility.

Key Responsibilities

• Design, build, and maintain clinical trial databases (eCRFs) using EDC systems.
• Develop data management plans and contribute to study protocols.
• Oversee data cleaning activities, including query generation and resolution.
• Ensure compliance with data management best practices, SOPs, and regulatory requirements (e.g., GDPR, ICH).
• Collaborate with biostatisticians and programmers to ensure timely database lock and data transfer.

Requirements

• Bachelor's degree in a relevant scientific or technical field.
• Minimum of 4 years of experience in clinical data management, with strong knowledge of EDC systems (e.g., Medidata Rave, Oracle Clinical).
• Proficiency in database design, data validation, and data reconciliation processes.
• Understanding of clinical trial processes and regulatory guidelines.
• Excellent analytical, problem-solving, and communication skills.

Benefits

• Competitive salary and benefits package, including health insurance and pension.
• Generous annual leave allowance.
• Opportunities for professional development and certifications.
• Hybrid working model, blending office-based collaboration in Norwich with remote work.
• Be part of a team contributing to life-saving therapies.