As a Clinical Trial Project Planner, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
En tant que Planificateur de projets d’essais cliniques, vous vous joindrez à la plus grande et la plus complète organisation de recherche clinique au monde, propulsée par l’intelligence en santé.
What you will be doing:
* Identify and raise schedule conflicts, risks, and resource peaks/troughs appropriately for resolution.
* Participate in and contribute to cross-functional and functional teams to discuss, review, and optimize protocol/project/program schedules and study cost estimates.
* Participate in and contribute to cross-functional and functional teams to discuss, review, and optimize protocol/project/program schedules and resource management plans.
* Monitor project activities towards the next milestone, anticipate variances, support critical path analyses, and collaborate with the Asset PM, Clinical Operations, and project team to identify solutions to schedule risks.
* Perform scenario planning of project timelines across protocols and therapeutic areas to optimize resource use and ensure efficient delivery of milestones.
* Contribute to the validation of resource information at the project level with the team.
En quoi consistera votre travail:
* Identifier et soulever les conflits de calendrier, risques, et pics/creux de ressources pour résolution.
* Participer et contribuer aux équipes pour discuter, examiner, et optimiser les calendriers et estimations des coûts des études.
* Participer et contribuer aux équipes pour discuter, examiner, et optimiser les plans de gestion des ressources.
* Suivre l’évolution des activités du projet, anticiper les écarts, aider à analyser le chemin critique, et collaborer pour identifier des solutions aux risques de calendrier.
* Planifier les échéances des projets pour une utilisation optimale des ressources et une réalisation efficace des étapes.
* Valider les informations sur les ressources avec l’équipe du projet.
You are:
Education
* Bachelor’s degree or higher.
* S. with 5+ years' experience or M.S. with 3+ years' experience.
Experience
* At least 3 years in project planning and management.
* Experience in the pharmaceutical industry or similar sector.
Beneficial Relevant Capabilities
* PMP certification preferred but not required.
* Experience in regulatory submission planning and product launch planning.
* Experience with planning and resource forecasting tools (e.g., MS Project, Planisware, OnePager).
Vous possédez:
Formation:
* Diplôme de niveau baccalauréat ou équivalent.
* Maîtrise en sciences avec 3 à 5 ans d’expérience.
Expérience:
* Minimum 3 ans en planification et gestion de projets.
* Expérience dans l’industrie pharmaceutique ou secteur similaire.
Compétences utiles:
* Certification PMP souhaitée mais non requise.
* Expérience en planification réglementaire ou lancement de produits.
* Maîtrise des outils de planification et de prévision des ressources.
What ICON can offer you:
Our success depends on the quality of our people. We’ve built a diverse culture rewarding high performance and nurturing talent.
In addition to a competitive salary, we offer benefits focused on well-being and work-life balance, including:
* Annual leave entitlements
* Health insurance options
* Retirement planning options
* Global Employee Assistance Programme (TELUS Health)
* Life assurance
* Optional benefits like childcare vouchers, gym discounts, etc.
Visit our careers site for more: https://careers.iconplc.com/benefits
ICON is committed to inclusion and accessibility. All qualified applicants will be considered without discrimination. For accommodations, contact us via: https://careers.iconplc.com/reasonable-accommodations
We encourage you to apply even if you do not meet all requirements; you might be exactly what we’re looking for.
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