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Clinical Trials Data Manager

2 months ago


London, Greater London, United Kingdom University College London Hospital Full time

The use of artificial intelligence is monitored, and applicants who have used it are required to declare this in their supporting statement.

The Cancer Clinical Trials Unit at University College London Hospital is seeking a Data Manager to support a portfolio of Phase I-III clinical trials within the Myeloma team - Haematology. The successful candidate may be required to cover other disease areas on a short-term or longer-term basis.

The post-holder will be responsible for delivering and verifying trial-specific information to sponsors, supporting the team with the set-up of new clinical trials, and assisting with the processing of biological samples, among other tasks.

You will be part of a supportive and dynamic team, working closely with clinical research staff. While the position is administrative, the role is vital in supporting clinical research staff deliver excellent care to patients with cancer.

We are currently supporting hybrid remote working, allowing a combination of working from home and office-based working. Flexibility around on-site working is essential, and you may be required to attend the office at relatively short notice to ensure that the service is covered.

We are looking for someone with experience of clinical research, knowledge of cancer, good verbal and written communication skills, and some experience of working in a healthcare setting. The ideal candidate will lead on data entry, processing updated information and documents for the successful running of the study, processing lab samples, and liaising with support departments to obtain tumour block samples, scan reports, and other vital information.

Key responsibilities include:

  • Leading on data entry and processing updated information and documents for the successful running of the study
  • Processing lab samples and liaising with support departments to obtain tumour block samples, scan reports, and other vital information
  • Supporting the team with the set-up of new clinical trials
  • Delivering and verifying trial-specific information to sponsors

Requirements:

  • Life Science degree
  • Knowledge of the drug development process and concept of clinical trials
  • Knowledge of oncology and/or haematology
  • Experience of working under minimal supervision
  • Experience of independently carrying out a research project
  • Experience of conducting clinical trials
  • Computer literacy, including experience of Word and Excel
  • Proven ability to communicate effectively in writing
  • Ability to identify own training needs
  • Displays desire for professional and personal development