Tasks:
* Ensure regulatory and GxP/GEP compliance;
strong understanding ofRA/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: 12/2025
Duration: 12 months
Capacity: 4 days per week
Location: remote