Do you enjoy working as a Clinical Research Associate and want to build further on your experience? Don't hesitate and apply today for this Clinical Research Associate position in a dynamic, international and familial company!
Job Description
As a Clinical Research Associate 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.
Responsibilities
- You conduct and report SIV, RMV, COV onsite monitoring visits
- You perform CRF review, source document verification and query resolution
- You are responsible for site communication and management
- You are a point of contact for in-house support services and vendors
- You communicate with internal project teams regarding study progress
- You participate in feasibility research
- You provide support to the regulatory team in preparing documents for study submissions
- You prepare and participate on audits and inspections
Requirements
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent on-site 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 English, Dutch and French
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Existing right to work in Europe required
Benefits
- A balanced salary package based on your capabilities and experience, including extra legal benefits
- As a CRA you will have a great flexibility between office work and remote work
Vacancy number: 18741
