
Clinical Trial Project Planner
3 semanas atrás
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 progress of project activities towards the next milestone, anticipate and highlight variances, support critical path analyses, and partner with the Asset PM, Clinical Operations, and the project team to identify solutions to schedule risks.
- Perform scenario planning of project timelines within and 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 les résoudre;
- Participer et contribuer aux équipes pour discuter, examiner et optimiser les calendriers et estimations des coûts;
- 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;
- Contribuer à la validation des informations sur les ressources au niveau du projet.
You are:
Bachelor's degree or equivalent with 5+ years' experience, or Master's with 3+ years' experience.
Experience in project planning, project management, and the pharmaceutical industry.
Beneficial skills include PMP certification and experience with planning tools.
Vous possédez:
- Diplôme de niveau baccalauréat ou maîtrise en sciences avec 3-5 ans d'expérience.
- Expérience en gestion de projets et dans l'industrie pharmaceutique.
- Compétences en planification et en gestion des ressources, certification PMP souhaitée.
What ICON can offer you:
- Competitive salary and benefits including health insurance, retirement plans, and work-life balance initiatives.
- A diverse and inclusive work environment committed to equal opportunities.
Visit our careers website for more information: https://careers.iconplc.com/benefits
ICON is dedicated to inclusion & belonging, providing accommodations for applicants with disabilities. Learn more at https://careers.iconplc.com/reasonable-accommodations
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