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Site Contract Specialist II
PSI CROLeuven, Flanders, Belgium1 dag geleden
FunctieomschrijvingCollege / University degree in Life Sciences or an equivalent combination of education, training and experience At least 3 years of full-scope Study Startup experience in Belgium Full professional working proficiency in Dutch and English Well-developed communication and organizational skills Ability to negotiate and build relationships at all levels
Job Description
Join our international team and be the key support to clinical research projects, part of the start-up team, working in a dynamic multi-functional environment, gaining unique skills from various disciplines relevant to clinical research.
This is a hybrid work arrangement that combines working from our Leuven office with the option to work from home.
You will :
- Review and negotiate site budgets
- Facilitate the review and negotiation of clinical trial agreements (CTAs) and investigator grants between PSI Legal, the project team, and the study site
- Customize and prepare contractually binding site-specific documents in cooperation with PSI Legal
- Track CTA and investigator grant negotiation status in the Clinical Trial Management System (CTMS)
- Prepare the executable version of the contract, including grants, and coordinates the signature process
- File executed contracts in the Trial Master File and maintains local documentation
- Liaise with the project team, translation, and legal departments on site contracting and grant negotiation matters
Qualifications
Additional Information
Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.
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Specialist Contract • Leuven, Flanders, Belgium