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 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 milestones, anticipate variances, support critical path analyses, and partner with the Asset PM, Clinical Operations, and project teams 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 validating 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, anticiper les écarts, analyser le chemin critique, et collaborer pour identifier des solutions aux risques liés au calendrier.
- Planifier les échéances entre protocoles et domaines thérapeutiques pour une utilisation optimale des ressources.
- Valider les informations sur les ressources avec l’équipe du projet.
You are:
Education
- Bachelor’s degree, with 5+ years' experience, or Master’s degree with 3+ years' experience.
Experience
- At least 3 years in project planning and management.
- At least 3 years in the pharmaceutical industry or a similar field.
Beneficial Capabilities
- Project Management Professional (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 maîtrise en sciences avec 3-5 ans d’expérience.
Expérience:
- Au moins 3 ans d’expérience en gestion de projets dans l’industrie pharmaceutique ou similaire.
Compétences utiles:
- Certification PMP souhaitée mais pas obligatoire.
- Expérience en planification réglementaire ou de lancement de produits.
- Expérience avec outils de planification et de prévision des ressources.
What ICON can offer you:
Our success depends on our people. We value diversity, high performance, and talent development. We offer a competitive salary, comprehensive benefits, and opportunities for work-life balance, including health insurance, retirement plans, and wellness programs. Visit https://careers.iconplc.com/benefits to learn more.
ICON promotes an inclusive environment and is committed to equal employment opportunity. We provide accommodations for applicants with disabilities. For more information, visit https://careers.iconplc.com/reasonable-accommodations.