Spektrum supports apex purchasers (NATO, UN, EU, and National Government and Defence) and their Tier 1 supplier ecosystem with a wide range of specialist services. We provide our clients with professional services, specialised aerospace and defence
The Clinical Research Regulatory Coordinator is responsible (primarily or in supporting role) for all activities related to the submissions of clinical trials applications in the CTR online platform known as Clinical Trial Information System (CTIS). The submitted
What Youll Do: Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines
Deadline Date: Tuesday 15 September 2026 Requirement: Second Line Security Event Analyst Location: Mons, BE Full Time On-Site: Yes Time On-Site: 100% Total Scope of the request (hours): 395 Required Start Date: 26 October 2026 End