Clinical Trial Site Recruiter
il y a 7 jours
Our Company Overview
CareForce One is a leading global Contract Research Organization (CRO) with a presence in multiple therapeutic areas. We strive to optimize clinical trial progress through strategic partnerships with research sites.
Job Scope
You will be responsible for developing relationships with clinical research sites to advance clinical trial progress. Your expertise will be essential in maintaining internal site databases, creating initial lists of potential sites, and communicating with project teams to fine-tune strategy and methodology.
Main Responsibilities
- Collaborate with Study Startup, Clinical Operations, and Process Improvement teams to maintain and refine internal site databases.
- Develop and implement improvement strategies for the site identification process, including related training activities.
- Create initial lists of potential sites based on study objectives and optimal site profiles.
- Communicate with project teams to fine-tune strategy and methodology of initial and follow-up site contacts.
- Maintain a study site identification tracker for further site evaluation and selection activities.
Qualifications
- Master's degree in Life Sciences or equivalent combination of education, training, and experience.
- Minimum 3 years of proven prior experience in on-site monitoring activities or CRA roles.
- Full professional working proficiency in Dutch, English, and French.
- Understanding of Good Clinical Practice, local laws, and applicable regulations in Belgium.
- Strong communication and collaboration skills.
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