Overview
As a Clinical Trial Project Planner, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
Responsibilities
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 progress of project activities towards milestones, anticipate and highlight potential variances, support critical path analyses, and partner with the Asset PM, Clinical Operations, and project team to identify/recommend solutions to schedule risks.
- Perform scenario planning of project timelines within and across protocols and therapeutic areas to optimize resource utilization and ensure efficient milestone delivery.
- Contribute to validating resource information at the project level with the project 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 interfonctionnelles pour discuter, examiner, et optimiser les calendriers et estimations des coûts.
- Participer et contribuer aux équipes pour discuter, examiner, et optimiser les plans de gestion des ressources.
- Suivre l’évolution des activités du projet, anticiper et mettre en évidence les écarts, analyser le chemin critique, et collaborer pour identifier des solutions aux risques liés au 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.
Qualifications
You are:
Education
- Bachelor's degree or equivalent.
- 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 Capabilities
- Project Management Professional (PMP) certification preferred.
- Experience with regulatory submission planning and product launch planning.
- Familiarity 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 3-5 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.
What ICON can offer you:
Our success depends on our people. ICON offers competitive salaries, benefits focused on well-being and work-life balance, including health insurance, retirement plans, employee assistance programs, and more. Visit our careers website for details: https://careers.iconplc.com/benefits
ICON values inclusion & belonging, providing an accessible environment for all candidates. We are committed to non-discrimination and equal opportunity. If you need accommodations during the application process, please contact us via the provided link.