Clinical Trial Data Manager

Royal Papworth Hospital NHS Foundation Trust; Cambridge; On-site; GBP 80,000 - 100,000; Full time

Job summary

A reputable NHS foundation trust in Cambridge is seeking a Clinical Trial Data Manager to lead database systems for clinical trials. The ideal candidate will possess significant data management experience, expertise in clinical data systems, and a collaborative spirit to work with statisticians. This opportunity offers a key role in ensuring high-quality data throughout various trial stages, from protocol design to analysis.

Qualifications

• Significant data management experience in a clinical trial setting.
• Experience with designing electronic case report forms and data validations.
• Previous line management experience beneficial.

Responsibilities

• Design, implement, and maintain database systems for clinical trial data.
• Ensure compliance with regulatory requirements.
• Support design, monitoring, and analysis of data sets.

Skills

Clinical trial data management

Database design

Data analysis using R

Tools

Clinical data management systems

Job description

About us: Papworth's Trials Unit Collaboration (PTUC) and is based in the Heart and Lung Research Institute (HLRI), near Royal Papworth Hospital on the Cambridge Biomedical Campus. The Data Management (DM) team works within PTUC to generate high quality data for our trials.

About the role: This role is integral to the DM team, and it is an excellent opportunity to utilise your clinical trial data management skills in all study types, including CTIMPs, devices and multi-site studies. Being involved at all trial stages, from protocol design to database lock.

The post holder will be responsible for designing, implementing, and maintaining database systems and resources for the recording of clinical trials data, ensuring that they are compliant with appropriate regulatory requirements.

They will also work closely with PTUC's statisticians to provide support to the design, monitoring, and analysis of data sets (using R). Working as a liaison between the statisticians and the DM team, to improve data analysis.

About you: You will have significant data management experience, within a clinical trial setting. You will have experience of using clinical data management systems and designing electronic case report forms and data validations. Previous line management experience would be beneficial.