Sr Medical Advisor/ Mgr/Sr Mgr-KunTuo

IQVIA · Shanghai, China +1 more

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Medical AffairsFull-timeCompany career page

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Role summary

IQVIA seeks a senior medical advisor to support clinical trial operations across sites in Shanghai and Beijing. Responsibilities include organizing investigator meetings, preparing medical documentation, conducting protocol reviews, designing monitoring plans, and providing medical training. Candidates need clinical trial expertise, regulatory knowledge, strong communication skills, and 1–3 years of relevant experience depending on educational background.

What they're looking for

Clinical medicine bachelor's degree or pharmacy-related master's degree minimum
3+ years medical advisor or clinical research experience with bachelor's degree
Knowledge of clinical trial regulations including China GCP and ICH-GCP
Proficiency in Microsoft Word, PowerPoint, and Excel
Fluent English with strong oral and written communication abilities
Presentation and training skills
Strong teamwork and collaborative relationship-building capability

What you'll be doing

Organize clinical trial symposia and communicate with principal investigators and therapeutic area experts
Conduct medical writing for clinical protocols, summary reports, and related trial documents
Review study protocols, informed consents, investigator manuals, case report forms, statistical analysis plans, and adverse event coding
Develop medical monitoring plans to ensure project quality and safety oversight
Support clinical operations team including feasibility assessments and principal investigator selection

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Date posted30 days ago

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