Senior Clinical Research Associate
3 settimane fa
Job Summary
We are seeking a Senior Clinical Research Associate to join our Biotech team at ICON plc. As a Senior CRA, you will work independently and collaboratively to coordinate activities, set up and monitor studies, and ensure adherence to regulations and principles of ICH-GCP.
Key Responsibilities
- Coordinate activities to set up and monitor studies
- Complete accurate study status reports and maintain study documentation
- Submit protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions
- Participate in preparing and reviewing study documentation and feasibility studies
- Balance sponsor generated queries efficiently and responsible for study cost-effectiveness
Requirements
- Minimum of 2.5 years independent monitoring experience in phase I-III trials as a CRA
- Knowledge of ICH-GCP guidelines and expertise to review and evaluate medical data
- Excellent written and verbal communication in English and Italian
- Ability to produce accurate work to tight deadlines within a pressurized environment
- Valid driving license
What We Offer
At ICON plc, we offer a competitive salary, a range of health insurance offerings, competitive retirement planning, and a global Employee Assistance Programme. We also offer flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, and discounted gym memberships.
Equal Opportunities
ICON plc is an equal opportunity and inclusive employer, committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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