Site Contract Specialist II
Site Contract Specialist II
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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 :
- College/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
Additional Information :
Advance your career in clinical research coordinating a variety of tasks and learning new things while growing with the company.
Remote Work :
No
Employment Type :
Full-time
Employment Type
Full-time
