Role Responsibility
You will coordinate and manage the activities of the studies, costs and project
team to agreed timelines adhering to SOP¡¯s and ICH-GCP. You will liaise with
Resource Management and the CRA Line Management team to make sure your allocated
resources are effective and meet the project needs.
In addition, your main tasks include
• Manage multi service projects globally or regionally as required. Managing
the sponsors' expectations and the relationship to deliver the projects on
time and in budget.
• Develop and manage project plans and study budgets ensuring targets are
met through regular review and tracking whilst monitoring quality metrics
so standards are maintained.
• Effectively communicate and collaborate with Business Development,
Finance, Management and Sponsor for change orders and other relevant
activities, revenue recognition and status progress. Proactively address
change in scope with the sponsor.
• Develop suitable plans to accommodate changes to project team and
monitor workload of project team ensuring sufficient project resource is
allocated at the difference stages of the project.
• Take a role in the development of new Project Managers within ICON.
• Participate and in some cases lead bid defence proposals for the company.
• Oversee the governance of each assigned project and escalate critical
issues as required.
• Participate in Out of Hours on-call rota as required.
Experience and Qualification
• You will have a University/Bachelors Degree in medicine, science or
equivalent and at least 2 years experience as a Clinical Project Manager.
You will demonstrate a satisfactory progression of monitoring and relevant
people management experience showing a good understanding of project
management processes with medium sized or international studies. In
addition you will also require:
• Excellent Project Management skills, with a proven track record of
managing clinical projects across regions.
• Strong communication and highly developed problem solving skills.
• You will have a in-depth understanding of drug development with good
commercial/clinical awareness and customer focus and a thorough
knowledge of ICH-GCP and relevant regulations for the conduct of clinical
trials.
• Fluent in written and spoken English as well as the local language of the
country to which you apply, your ability to interact with clients and all
levels of staff will enable you to build successful working relationships.
• You must have the ability to travel at least 35% internationally and
domestic fly and drive and possess a full clean driver¡¯s license.
having 3-4 global project management experience
´ã´çÀÚ: ¿À¼ø¿µ
¿¬¶ôó: 010-6306-6801
À̸ÞÀÏ: sonia.oh@docsglobal.com
Á¦Ãâ¼·ù: ¿µ¹®À̷¼