Tasks
Ensure regulatory and GxP / GEP compliance; strong understanding of RA / MOH requirements and protocol implementation across regions.
Plan, execute, and close clinical projects within scope, time, and budget; build timelines and manage risks, resources, and milestones.
Oversee budget forecasting, burn rate monitoring, and scope change control.
Lead cross‑functional teams (Clinical, Epi, DM, Stats, Reg, PVG) and foster collaboration and accountability.
Communicate clearly with sponsors, vendors, and stakeholders; translate complex requirements into actionable steps.
Anticipate issues, develop mitigation strategies, and adapt to regulatory or operational changes.
Qualifications
3+ years cross‑functional clinical PM experience
Strong regulatory / GEP and RA / MOH knowledge
Protocol interpretation across regions
End‑to‑end project delivery; risk, resource & milestone management
Study plan development; proficient with PM tools
Budget forecasting, burn‑rate & scope control
Clear stakeholder communication & actionable guidance
Risk anticipation, adaptability & solution‑oriented approach
Requirements
Start: 12/2025
Duration: 12 months
Capacity: 4 days per week
Location: remote
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