Do you have experience in Clinical Contracts and Budgets management with sites and want to extend and share your experience in a growing, dynamic, global company with a very nice familial team spirit? Don't hesitate and apply now Job Description As a Study Start-Up Specialist, you will be providing direct operational support to project teams and ensure that clinical projects start smoothly and on time. ResponsibilitiesDevelop and negotiate site contracts and budgetsCollect, review, and submit documents for ethics and regulatory review and approvalPrepare packages of site documents for drug release to clinical sitesCommunicate with project teams, investigative sites, review bodies, vendors, and clients regarding start up matters till the moment of site activationMonitor start up metrics and timelinesSupport site identification and selection processRequirementsCollege/University degree or an equivalent combination of education, training and experienceAy least 2 years full-scope study start up experienceC2 level in Dutch, full working proficiency in English and FrenchAbility to negotiate and build relationships at all levelsAbility to plan, multitask and work in a dynamic team environmentExcellent communication and collaboration skillsBenefitsFull-time position.Hybrid working policy (3 days/week home-based)A balanced salary package based on your capabilities and experience, including extra-legal benefits.