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.