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Sr. Staff Clinical Technical Program Manager, APAC

Dexcom · Singapour

New
Senior 🇬🇧 English
Microsoft Excel Microsoft Project Smartsheet GCP

Job description

About the role

Dexcom, a global leader in continuous glucose monitoring, is looking for a Senior Staff Technical Program Manager to lead planning and execution of complex clinical programs across the Asia Pacific region. The role supports product development, regulatory submissions and business objectives through multi-country studies, working with Executive Management, Product Development, Regulatory Affairs, Quality, Operations and external CROs.

Key responsibilities

  • Lead clinical studies from protocol design and startup through execution, closeout and reporting
  • Manage study operations: timelines, milestones, budgets, financial tracking, KPIs and performance metrics
  • Coordinate and prioritize activities across multiple studies and mitigate risks in enrollment, compliance, data quality and study success
  • Select, onboard and manage CROs and vendors through competitive bids and performance oversight
  • Oversee CRO deliverables, ethics committee submissions, site initiation visits, site training, monitoring and data integrity reviews
  • Maintain study documentation such as Clinical Investigation Plans, Informed Consent Forms and Case Report Forms
  • Build dashboards, executive reports and portfolio updates for leadership
  • Drive process improvements and support studies in Australia, New Zealand, Japan, Korea, Singapore and other APAC locations

Required profile

  • Bachelor's degree in a technical discipline and 13+ years of related experience, or a Master's degree and 8+ years, or a PhD and 5+ years
  • Knowledge of clinical research regulations and GCP; experience in medical devices, biotechnology, pharmaceuticals or healthcare technology
  • Experience planning, managing and executing clinical studies, including multi-country programs
  • Comfortable across APAC and U.S. time zones and willing to travel regionally (25-50% travel required)

Nice-to-have qualifications

  • Managing CROs for Class II and Class III medical device studies
  • Support for diabetes, digital health or glucose monitoring device studies
  • Working knowledge of clinical research practices in APAC markets
  • Process improvement experience

Required skills

  • Microsoft Excel, Word, PowerPoint, Microsoft Project and Smartsheet
  • Project management, risk assessment, stakeholder management and communication

What we offer

  • Comprehensive benefits program
  • Growth opportunities and career development through in-house learning programs and/or tuition reimbursement

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Published 2 hours ago

Expires 1 month from now

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Dexcom

Singapour