As a Clinical Research Associate at PSI 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.
You will:
- 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
Qualifications :
- College/University degree in Life Sciences or an equivalent combination of education training & experience
- Independent onsite monitoring experience in France
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in oncology hemophilia infectious diseases GI
- Full working proficiency in English and French
- Proficiency in MS Office applications
- Ability to plan multitask and work in a dynamic team environment
- Communication collaboration and problemsolving skills
- Ability to travel
Additional Information :
This is a great opportunity for you to further develop your skills widen your therapeutic area experience and become an expert in clinical research.
We offer:
- Big professional advancement opportunity within Clinical Operations with specific mentorship and training program
- Development opportunities across PSI departments
- Flexible working hours
- Homeoffice option available as well as combination of home and office work arrangement
- Extensive onboarding trainings and professional development training programs
- Highly developed company culture and positive team atmosphere
- Additional leave days (12 days of RTT)
Remote Work :
Yes
Employment Type :
Fulltime