
Clinical Research Associate II
- Milano
- Tempo indeterminato
- Full time
- Conduct and report all types of onsite monitoring visits
- Be involved in study startup
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be a point of contact for in-house support services and vendors
- Communicate with internal project teams regarding study progress
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
- Prepare for and participate in audits and inspections
- University/College degree in Life Sciences or an equivalent combination of education, training & 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
- Communication, collaboration, and problem-solving skills
- Ability to travel
- PSI is a stable, privately-owned company, organically growing since 1995.
- We have an excellent reputation in the industry, having won the CRO Leadership awards several years in a row.
- Team collaboration is high on our agenda. Our aim is for employees to feel valued and heard in friendly and supportive teams.
- We offer extensive onboarding and mentorship programs, profound therapeutic area trainings, interactive soft-skills trainings.
- PSI CRAs have an opportunity to work with different Sponsors on a variety of therapeutic areas.