As a CRA II in Switzerland, you will be joining the world's largest and most comprehensive clinical research organisation, powered by healthcare intelligence.
You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people's lives. Working in this program, you will feel challenged and supported to advance in your professional career while making a meaningful impact.
Key Responsibilities:
* Conduct independent and proactive work to set up and monitor studies, complete reports, and maintain documentation
* Submit protocol, consent documents for ethics/IRB approval, as well as prepare regulatory submissions
* Take responsibility for study cost efficiency
* Prepare and review study documentation and feasibility studies for new proposals
* Potential to assist in training and mentoring fellow CRAs
Requirements:
* At least 2 years of monitoring experience in phase I-III trials as a CRA
* Degree in medicine, science, or equivalent
* Previous monitoring experience in medium-sized studies, including study start-up and close-out
* Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
* Excellent written and verbal communication skills in German and French or Italian
* Ability to work to tight deadlines
* Availability to travel at least 60% of the time (international and domestic) and possess a valid driving license
About ICON:
We value our employees and strive to create a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of benefits to support your well-being and work-life balance.
* Varying annual leave entitlements
* A range of health insurance options
* Competitive retirement planning offerings
* Global Employee Assistance Programme
* Life assurance
* Flexible country-specific optional benefits
We are committed to diversity, inclusion, and belonging, and we strive to provide an inclusive and accessible environment for all candidates.