Clinical Research Associate II
5 giorni fa
Job Overview
As a Clinical Research Associate II at PSI, you will play a vital role in ensuring the highest quality standards in clinical studies. Your responsibilities will include conducting and reporting onsite monitoring visits, participating in study startup, and performing CRF review and query resolution.
Key Responsibilities
- Conduct and report onsite monitoring visits to ensure compliance with regulatory requirements
- Participate in study startup activities, including site selection and feasibility research
- Perform CRF review and source document verification to ensure data accuracy
- Communicate with internal project teams regarding study progress and site management
- Support regulatory team in preparing documents for study submissions
- Prepare for and participate in audits and inspections to ensure compliance
Requirements
- University/College degree in Life Sciences or an equivalent combination of education, training, and experience
- At least 2 years of independent on-site monitoring experience in Italy
- Experience in all types of monitoring visits in Phase II and/or III
- Full working proficiency in English and Italian
- Proficiency in MS Office applications
- Ability to plan, multitask, and work in a dynamic team environment
About PSI
PSI is a stable, privately-owned company with an excellent reputation in the industry. We offer a supportive team environment, extensive onboarding and mentorship programs, and opportunities for professional growth and development.
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