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Search Results for Clinical Research Associate
Job Title. Location Salary Actions

eClinical Project Coordinator

eClinical Project Coordinator Our client, a growing, innovative healthcare technology are currently recruiting for an eClinical Project Coordinator to join their team on a permanent basis. Remote working is an option with this opportunity. As Project Coordinator you will support the project team in the strategic planning and implementation of overall project plans, scopes, and schedules-ensuring deliverables are made on time and within project budget. As Project Coordinator you will be instrumental in the delivery of prod...

Location: Republic of Ireland,
eClinical Project Coordinator
Republic of Ireland Not Disclosed

eClinical Project Manager

eClinical Project Manager Our client, a growing, innovative healthcare technology are currently recruiting for an eClinical Project Manager to join their team on a permanent basis. Remote working is an option with this opportunity. As eClinical Project Manager you will plan, lead and maintain the overall delivery of the organisations products and services for clinical research studies. As Project Manager (PM) you will be detail-oriented, customer focused and clinical research experienced team member. You will focus on project plans/timelines, risk mitigation, action item...

Location: Republic of Ireland,
eClinical Project Manager
Republic of Ireland Not Disclosed
Other Clinical Research Jobs
Job Title Location Salary Actions
Project Scheduler Limerick Not Disclosed

Clinical Research Associate Career Profile

Clinical Research Associate


The Clinical Research Associate is tasked with monitoring clinical trials sites in order to ensure that studies are carried in accordance with the study protocol, the company standard operating procedures (SOP), applicable regulations and the principles of ICH - GCP (International Conference on Harmonisation - Good Clinical Practice).

Key Responsibilities


  • Identification of key investigators
  • Assistance in the preparation of regulatory submissions
  • Design patient information sheets and consent forms
  • Coordinate document translation and verification
  • Ensure timely submission of protocol/consent documents/safety reports for Ethics/IRB approval according to local requirements
  • Pre-study and initiation visits
  • Conduct regular monitoring visits in accordance with the trial site monitoring SOP
  • Maintain all files and documentation pertaining to studies
  • Motivate investigators in order to achieve recruitment targets
  • Complete accurate study status reports.
  • Ensure the correct storage of drugs and the diligent account of all drugs in accordance with SOPs
  • Keep the project manager regularly informed
  • Process case record forms to the required quality standards and timelines
  • Ensure the satisfactory close-out of investigator sites
  • Ensure correct archiving of files on completion of a study
  • Co-operate with QA personnel in the conduct of QA audits
  • Participate in feasibility studies for new proposals
  • Maintain patient confidentiality

Qualifications / Experience Required


  • Degree in Life Sciences or Equivalent
  • Ability and willingness to travel at least 50% of the time, both international and local
  • Ability to review and evaluate clinical data
  • Computer literacy desirable
  • Foreign language skills desirable
  • Current full driving license essential
  • Good oral and written communication skills