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 approachRequirements:Start: asapDuration: 12 monthsCapacity: 2-3 days per weekLocation: remote