Job Title

As a Clinical Trial Project Planner, you will be joining the worlds largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:Identifies and raises schedule conflicts, risks, and resource peaks/troughs appropriately for resolution.Directly participates in and contributes to cross-functional and functional teams to discuss, review, and optimize protocol/project/program schedules and study cost estimates.Directly participates in and contributes to cross-functional and functional teams to discuss, review, and optimize protocol/project/program schedules and resource management plans.Monitors progress of project activities towards next project milestone, anticipates and highlights potential variances, supports line/team in critical path analyses and understanding the impact, and partners with the Asset PM, Clinical Operations, and the project team to identify/recommend solutions to schedule risk.Performs scenario planning of project timelines within and across protocols and across therapeutic area/portfolio to enable optimum use of local, global, and outsourced resources to ensure efficient delivery of project milestones.Contributes to the validation of resource information at the project level with the project teamEn quoi consistera votre travail :Identifier et soulever les conflits de calendrier, les risques et les pics/creux de ressources de manire approprie pour les rsoudre;Participer et contribuer directement au travail des quipes interfonctionnelles et fonctionnelles afin de discuter, dexaminer et doptimiser les calendriers des protocoles/projets/programmes et les estimations des cots des tudes;Participer et contribuer directement au travail des quipes interfonctionnelles et fonctionnelles afin de discuter, dexaminer et doptimiser les calendriers des protocoles/projets/programmes et les plans de gestion des ressources;Suivre lvolution des activits du projet en vue de la prochaine tape, anticiper et mettre en vidence les carts potentiels, aider la branche/lquipe analyser le chemin critique et en comprendre limpact, et collaborer avec le GP des actifs, les oprations cliniques et lquipe du projet pour identifier/recommander des solutions aux risques lis au calendrier;Planifier les chances des projets lintrieur et entre les protocoles ainsi quentre les domaines thrapeutiques et le portefeuille pour permettre une utilisation optimale des ressources locales, mondiales et externalises afin dassurer une ralisation efficace des tapes du projet;Contribuer la validation des informations sur les ressources au niveau du projet avec lquipe du projet. You are:EducationBachelors level degree.S. with 5+ years' experience or M.S. with 3+ years' experience. ExperienceAt least 3 years experience in project planning and project management.At least 3 years of applicable pharmaceutical industry experience or similar industry experience. Beneficial Relevant CapabilitiesProject Management Professional (PMP) certification preferred but not required.Experienced in end-game/regulatory submission planning and/or product launch planning.Experienced with planning and resource forecasting tools (e.g., MS Project, Planisware, OnePager).Vous possdez : Formation :Diplme de niveau baccalaurat;Matrise en sciences avec 5 ans dexprience ou matrise en sciences avec 3 ans dexprience ou plus. Exprience :Au moins 3 ans dexprience dans la planification et la gestion de projets;Au moins 3 ans dexprience dans lindustrie pharmaceutique ou dans un secteur similaire. Comptences utiles :Certification de professionnel de la gestion de projet (PMP) souhaite mais non requise;Exprience dans la planification des envois finaux/rglementaires et/ou de la planification des lancements de produits;Exprience des outiWhat ICON can offer you:Our success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Our benefits examples include:Various annual leave entitlementsA range of health insurance offerings to suit you and your familys needsCompetitive retirement planning offerings to maximise savings and plan with confidence for the years aheadGlobal Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your familys well-beingLife assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among othersVisit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefitsAt ICON, inclusion & belonging are fundamental to our culture and values. Were dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodationsInterested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless theres every chance youre exactly what were looking for here at ICON whether it is for this or other roles.