Job Summary
We are seeking a highly motivated and experienced Clinical Research Associate II to join our team in Switzerland. As a key member of our clinical research organization, you will be responsible for partnering with pharmaceutical companies to advance the development of treatments that improve and save lives.
Key Responsibilities:
* Independently manage study setup and monitoring, complete reports, and maintain accurate documentation.
* Submit protocol and consent documents for ethics and IRB approval, as well as prepare regulatory submissions.
* Ensure study cost efficiency and take responsibility for budget management.
* Develop and review study documentation, feasibility studies, and new proposal proposals.
* Support training and mentoring of fellow CRAs, enhancing their skills and knowledge.
Your Profile:
* A minimum of 2 years of monitoring experience in phase I-III trials as a CRA.
* A degree in medicine, science, or equivalent.
* Prior experience in medium-sized studies, including study start-up and close-out.
* Familiarity with ICH-GCP guidelines and ability to review and evaluate medical data.
* Excellent written and verbal communication skills in German, French, or Italian.
* Ability to work under tight deadlines and adapt to changing priorities.
* Availability to travel at least 60% of the time (domestic and international) and possession of a valid driving license.
About ICON:
We prioritize building a diverse culture that rewards high performance and nurtures talent. Our competitive salary and benefits package includes various annual leave entitlements, range of health insurance offerings, retirement planning options, and more.
Inclusive Work Environment:
* Diversity, inclusion, and belonging are fundamental to our culture and values.
* We strive to create an inclusive and accessible environment for all candidates.
* We are committed to providing a workplace free from discrimination and harassment.