Are you an experienced CRA with a high interest in Feasibility? Don't hesitate and apply now! You will be welcomed in a global company in which team spirit is key.
Job Description
As a Site Identification Specialist, you will be dedicated to developing strategic relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials.
Responsibilities
- Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement
- Participate in the development of improvement strategies for the site identification process, implementation thereof, as well as related training activities
- Define the main study objectives and the optimal site profile
- Create initial list of potential sites
- Communicate with project teams on project/ regional level to fine-tune strategy and methodology of initial and follow-up site contacts depending on indication, regional specifics, and technologies in use
- In cooperation with the project team, maintain a study site identification tracker for further site evaluation and selection activities
- Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives
- In cooperation with Legal, perform due diligence check of regulatory and legal limitations applicable to the recommended investigators or clinical sites
- Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/investigator is needed
Requirements
- University/college degree (Life Sciences/Pharmacy/Healthcare field is a plus), or an equivalent combination of education, training and experience
- Minimum 4 years of proven prior experience in on-site monitoring activities
- Sales driven and result-oriented
- Full professional working proficiency in Dutch and English, professional proficiency in French is an asset and needed to communicate with French speaking sites
- Understanding of Good Clinical Practice, local laws and applicable regulations in Belgium and the Benelux region
- Communication and collaboration skills
- Demonstrated ability to work in a dynamic environment, under compressed deadlines across several projects, each with unique requirements
- Experience in oncology, hematology or IBD is a plus
Benefits
- Full time position
- Indefinite duration contract
- A balanced salary package based on your capabilities and experience, including extra legal benefits
Vacancy number : 25741
