Director Clinical Program Management

Job content

Summary Of Responsibilities

This person will help coordinate the efforts of extended team members, notably the scientific study leader (epidemiologist for observational studies, Medical Affairs Leader for interventional studies). This position may own specific areas or deliverables within a study, or in some cases, assume the accountabilities of a team leader for study delivery.

• Management of study Governance processes
• Management of internal and external stakeholders
• Finance Management support
• Project Management of owned study areas to deliver according to cost, time and quality
• Support of study Risk Management and Quality Management activities
• Study compliance
  

Education, Qualifications, And Experience

• Bachelor’s degree required preferably in medical or biological science or equivalent by experience.
• Extensive pharmaceutical industry within clinical study/research project delivery, drug development process and relevant guidelines, for example GCP/ICH, for a specific therapeutic and geographic area.
• Project Management qualification or demonstration of project management skills including scope, budget, timeline, resource management and use of associated tools.
• Scientific awareness and extensive knowledge of observational study guidelines and SOPs
• Extensive knowledge of early and late stage Pharmaceutical Development
• Ability to effectively work with CROs/External Providers.
• Proven ability to interact widely and effectively within the company across regions, functions and cultures.
• Experience within compliance management of Externally Sponsored Scientific Research
• Persuasive communicator with a proven ability to work collaboratively in a multi-cultural environment