As a Clinical Research Associate at PSI Italy you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.
Hybrid working arrangement in Milan area
Responsibilities:
- 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 inhouse 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
Qualifications :
- University/College degree in Life Sciences or an equivalent combination of education training & experience
- At least 2 years of independent onsite monitoring experience in Italy
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in Oncology / Gastroenterology therapeutic areas is a strong advantage
- 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 problemsolving skills
- Ability to travel
Remote Work :
No
Employment Type :
Fulltime