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Search Results for Clinical Data Manager
Job Title. Location Salary Actions

GCP Inspector

GCP Inspector Reporting to the GCP/Pharmacovigilance Inspection Manager, the role of the GCP Inspector is to evaluate the compliance of sites inspected, in Ireland and abroad, with the requirements of National legislation (in Ireland), European Community Directives, Regulations and Guidance. These sites may include: ·Sites where clinical trials are conducted ·Sites responsible for management, administration or data collection activities for clinical trials, (sponsor organisations, clinical research organisations) ·Clinical t...

Location: Dublin,
GCP Inspector 		Dublin Not Disclosed

Clinical Evaluator

Our client a European notified body for medical devices wishes to recruit a Clinical Evaluator for the review of medical devices and in vitro diagnostic devices. The Clinical Evaluator reports directly to the Chief clinical evaluator. This is a fantastic opportunity for a medical doctor looking for a career change to move into a fast growing and innovative sector Role/Responsibilities Responsible for the clinical assessment of technical documentation for Medical devices and In vitro diagnostic devices. Scientifically challenge and evaluate technical documentation pert...

Location: Republic of Ireland,
Clinical Evaluator 		Republic of Ireland Not Disclosed
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Clinical Data Manager Career Profile

Data Management


Clinical Data Management is concerned with the processing of incoming clinical trial data from ongoing trials and the analysis and organisation of the data in preparation for registration with the regulatory bodies, e.g. the Irish Medicines Board (IMB) or the US Food and Drug Administration (FDA).
The main entry level position in data management is the Clinical Data Coordinator and this position generally requires a good degree in life sciences or mathematics and a high competency in analytical and organisational skills.

Key Responsibilities


  • Migrate / deliver high quality data for specified protocols within agreed timeframes to achieve prompt submissions/publication of results
  • Write project procedures and guidelines for effective data capture and review in collaboration with clinical monitors
  • Ensure the quality of project data by developing and applying comprehensive validation procedures prior to the migration of data
  • Implement production databases at the start of each project to enable data cleaning to occur at an early stage; co-ordinate the design of record forms/screens for studies.
  • Communicate effectively with International Project team, and Corporate Computing Support
  • Provide training and support for Hospital Investigators and Study Staff; communicate effectively with investigational sites to resolve data clean-up queries
  • Maintain systems to track the data management process
  • Develop and maintain project data management plans and co-ordinate the activities of informal project data management teams comprising Clinical Research Officer(s), Data Entry, Data Analyst and external Contract Research Organisation staff to ensure adherence to agreed schedules