Ref #: 25754

Employment type: Permanent - Full-Time

Location: Belgium



* Ensure regional/global clinical operations deliverables progress according to agree upon timelines and milestones as leader of the Study Management Team (SMT). This includes country & site feasibility and site selection, trial set-up, study execution and trial closure and vendor set activities as assigned by the GTL
* Support GTL in leading related CRO country & site activities
* Study Management Team Leader
* Site selection, enrollment, monitor study progress
* Financial planning and tracking
* Document development
* Training and Investigator Meeting
* Cross functional Study Management
* Continuous Quality Focus
* Data Cleaning
* Participate in Global Clinical Development Initiatives as assigned
* Can act as Subject Matter Expert


* BS degree or equivalent required, preferably in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)
* Required: Minimum of 8 years clinical trial management experience in the pharmaceutical industry or CRO
* Experience with management and supervision of CROs/vendors is preferred.
* Clinical research operational knowledge, strong project planning/management and effective communication skills
* Strong analytical skills, and simultaneously demonstrates the ability to manage ambiguity when limited information is available
* Effective verbal and written communication skills leading to successful team collaboration
* Fluent English, Dutch and/or French a strong plus
* Proven experience in proactive planning, risk mitigating and gaining team consensus on updated plans during the project lifecycle
* Willing to travel internationally up to 20% of time