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

GCP/Pharmacovigilance Inspector

Our client is regulatory authority who are based in Dublin. They are seeking a GCP/ Pharmacovigilance Inspector to join an established team on a 2 year contract. Reporting to the GCP/Pharmacovigilance Inspection Manager, the role of an Inspector is to evaluate the compliance of sites inspected, both in Ireland and internationally, with the requirements of National legislation (in Ireland), European community directives, regulations and guidance. These include: Hospitals, Clinics, healthcare centres, clinical research facilities, sponsor organisations, CROs, C...

Location: Dublin,
GCP/Pharmacovigilance Inspector 		Dublin Not Disclosed

Director, Quality & Compliance (GCP)

Our client is a global Biopharma organisation who play a crucial role in developing life-saving therapies. They are seeking a Clinical Quality and Compliance Director who is ready to dive-in to support our clients clinical development programs. As a Clinical Quality and Compliance Director, you will support and work with our clinical study management teams and teammates across R&D Quality and Compliance. They need someone with strong leadership skills, expert Good Clinical Practice (GCP) knowledge, audit skills, communication, facilitation skills, and the ability to...

Location: Dublin,
Director, Quality & Compliance (GCP) 		Dublin Not Disclosed
Other Clinical Research Jobs
Job Title Location Salary Actions
Senior Project Manager Capital Projects Dublin 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