To assist with all technical and programming tasks for the data management of allocated projects:
To annotate the master CRF.
Having relevant past experience, within the pharmaceutical industry.
Expert in EDC systems programming such as Oracle InForm, RAVE and/or Oracle Clinical.
Good communication skills (oral and written) and good analytical skills.
Thorough knowledge of ICH Guidelines and GCP including regulatory requirements for the conduct of clinical development programs
Good project management skills.
Ability to inspire effective teamwork and motivate staff.
To assist with set up systems for study processing.
To prepare electronic data for export and prepare any documentation for return at study completion as requested.
To report progress against schedules to Project Manager or Lead Clinical Data Manager as appropriate.
To be aware of and to work to the standards appropriate to the study.
To perform quality control checks on programming outputs