Freelance Senior Clinical Research Associate
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Are you an experienced freelance CRA and have full-time availability for a project to start asap? You will be welcomed in a global company in which team spirit is key.
Job Description
As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Your focus will be on subjects' rights, safety and well-being and quality of data compliance.
Responsibilities
- Conducting and reporting all types of onsite monitoring visits
- Performing CRF reviews, source document verification and query resolution
- Be responsible for site communication and management
- Supervising study activities, timelines, and schedules for each site
- Acting as a point of contact for in-house support services and vendors
- Supporting quality control, such as compliance monitoring and reports review
Requirements
- BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
- Independent on-site monitoring experience in Belgium, ideally on multiple projects at a time
- Demonstrable experience in all types of monitoring visits in Phase II and/or III
- Experience supporting Oncology/ Hematology and Infectious disease studies
- Fluency in Dutch and English, with professional proficiency in French
- Full and clean driver's license, and the ability to travel
- Intermediate to Advanced knowledge of MS Office.
Contract Information
- Freelance opportunity
- Full-time (80% is not an option)
- Fully remote work + on-site visits
- 6 months contract
- Start-date : October the latest
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