IQVIA Asia Pacific
Position is virtual and will be working on UK / US hours. 8PM to 5am PH Time Experience in pharmaceutical or biotech project management and cross-functional team leadersh ipDemonstrated understanding of pharma quality and regulatory framewor k.Demonstrated success in matrix team environments with strong collaboration and accountabili tyFlexibility to work across global time zon esKnowledge of Good Manufacture Practice (GMP), Good Clinical Practice (GCP), and regulatory framewor ksProven ability to manage complex clinical development programs and multiple studi esStrong budgeting and forecasting skills, including supply demand planni ngSkilled in stakeholder alignment, negotiation, and performance measureme ntStrong interpersonal skills with a demonstrated ability to manage stakeholders in different levels of technical and business role s.Proven ability to effectively develop, communicate, and execute project plans with multiple stakeholder s.
IQVIA Asia Pacific
