As a Senior 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 SIV RMV COV onsite monitoring visits
- 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 and participate on audits and inspections
Qualifications :
- College/University degree in Life Sciences or an equivalent combination of education training & experience
- Independent onsite monitoring experience
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in Oncology is a plus
- Full working proficiency in Dutch and English
- Proficiency in MS Office applications
- Valid drivers license & ability to travel
Remote Work :
No
Employment Type :
Fulltime