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

Senior CRA

Senior CRA Role Responsibility Working within a highly qualified team you will identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV ensuring adherence to applicable regulations and principles of ICH-GCP. Additional Responsibilities: You will work independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol, consent documents...

Location: Dublin,
Senior CRA 		Dublin Not Disclosed

Clinical Trials Advisor

Clinical Trials Advisor Responsibilities: -Analysis of clinical trial protocols and other client source material -Build up a thorough knowledge of the trial -Preparation of study materials for development teams; -Determine what elements are important to the target audience and the depth of coverage required in the product -Script product content to meet client requirements and in-house quality Standards -Identify leverage from previous trials -Resolve clinical queries from the development teams -Storyboard with Graphic Designers as part of graphic development -Review and sign-off t...

Location: Limerick,
Clinical Trials Advisor 		Limerick Not Disclosed
All Clinical Research Jobs
Job Title. Location Salary Actions
Senior CRA Dublin Not Disclosed
Clinical Trials Advisor Limerick Not Disclosed
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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