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.
Qualification:
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: *******
Duration: 12 months
Capacity: 4 days per week
Location: remote