Site Activation Manager (evergreen)
IQVIA · Taipei City, Taiwan
Clinical OperationsFull-timeCompany career page
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Role summary
IQVIA seeks a Site Activation Manager to oversee clinical trial site activation, maintenance, and regulatory activities across assigned studies and multi-protocol programs. The role involves managing project delivery, regulatory strategy, documentation, and cross-functional coordination in a multi-regional environment.
What they're looking for
- Bachelor's degree in life sciences or related field
- 7+ years' experience in scientific or clinical environment, including international role
- Strong negotiation and communication skills with ability to challenge constructively
- In-depth knowledge of drug development process and regulated clinical trial environment
- Proficiency with GCP, ICH guidelines, and applicable regulatory frameworks
- Demonstrated ability to manage multiple complex projects with competing priorities
- Strong regulatory and technical writing skills
What you'll be doing
- Direct site activation, pre-award activities, and maintenance execution aligned with RSU strategy and project timelines
- Develop and maintain management plans, coordinate across regulatory and site activation functions, resolve project issues
- Identify regulatory complexity, assess regulatory landscape, determine strategy for submissions and authorizations
- Mentor colleagues, maintain CTMS and project tracking systems, lead client presentations and training
- Oversee multi-regional programs during startup and maintenance phases as study management team member
Privacy & handoff
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