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 : asap Duration : 12 months Capacity : 2-3 days per week Location : remote