We offer a full range of consulting, clinical development and commercialisation services from a global network of offices in 46 countries
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life.
We are a global provider of co...
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Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
Balancing sponsor generated queries efficiently, manage and support sites and responsible for study cost-effectiveness
Dependent on level of experience you may assist in training and mentoring less expert CRA’s
To be successful in the role, you will have:
At least 12 months of independent, on-site monitoring experience
Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
Great command of the local language and) English (command of any other languages will be considered an advantage
Ability to produce accurate work to tight deadlines within a pressurized environment
You will be asked to travel around 60% of the time domestically (on rare occasions internationally) and should possess a valid driving license
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