As a Clinical Trial Project Planner, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
What you will be doing:
- Identify and resolve schedule conflicts, risks, and resource peaks/troughs appropriately.
- Participate in and contribute to cross-functional teams to discuss, review, and optimize protocol/project/program schedules and study cost estimates.
- Participate in and contribute to cross-functional teams to discuss, review, and optimize schedules and resource management plans.
- Monitor project activities toward milestones, anticipate variances, support critical path analyses, and collaborate with the team to address schedule risks.
- Perform scenario planning of project timelines within and across protocols and therapeutic areas to optimize resource utilization and ensure timely delivery.
- Contribute to the validation of resource information at the project level with the project team.
En quoi consistera votre travail:
- Identifier et résoudre les conflits de calendrier, risques et pics/creux de ressources.
- Participer et contribuer aux équipes pour optimiser calendriers et estimations de coûts.
- Participer et contribuer aux équipes pour optimiser calendriers et plans de gestion des ressources.
- Suivre l’évolution des activités, anticiper les écarts, analyser le chemin critique, et collaborer pour proposer des solutions aux risques de calendrier.
- Planifier les échéances pour optimiser l’utilisation des ressources et respecter les jalons.
- Valider les informations sur les ressources avec l’équipe du projet.
You are:
Education
- Bachelor’s degree or equivalent.
- B.S. with 5+ years or M.S. with 3+ years of experience.
Experience
- At least 3 years in project planning and management.
- Experience in the pharmaceutical industry or similar sector for at least 3 years.
Beneficial Capabilities
- Project Management Professional (PMP) certification preferred but not required.
- Experience with regulatory submission planning and product launch planning.
- Proficiency with planning and resource forecasting tools (e.g., MS Project, Planisware, OnePager).
Vous possédez:
- Diplôme de niveau baccalauréat ou équivalent.
- Maîtrise en sciences avec 3 à 5 ans d’expérience.
Compétences utiles:
- Certification PMP souhaitée mais non requise.
- Expérience en planification réglementaire ou de lancement de produits.
- Compétence avec outils de planification et de prévision des ressources.
What ICON can offer you:
- Competitive salary and benefits focused on well-being and work-life balance.
- Various leave entitlements, health insurance, retirement plans, Employee Assistance Programme, and flexible benefits.
Visit our careers website for more details: https://careers.iconplc.com/benefits
At ICON, inclusion & belonging are core to our culture. We are committed to providing an accessible environment and equal opportunities for all applicants. For accommodations, please contact us through the provided link.