Oversee planning and execution of medium to large, regional or multi-regional RWE studies, ensuring speed, quality, and cost optimization
Serve as the primary point of contact for clients, fostering strong relationships and customer satisfaction
Drive cross‑functional integration across epidemiology, biostatistics, data science, medical affairs, regulatory, and vendor partners
Develop and implement integrated study management plans
Monitor project progress, mitigate and manage risks, and resolve issues proactively
Ensure compliance with GEP, GVP and local regulations (LGDP, LFPDPPP, PDPL, HIPAA, GDPR, and other country specific ethics requirements), and company processes
Manage project financials, including forecasting, scope changes, and revenue acceleration opportunities
Mentor and support team members, promoting continuous improvement and knowledge sharing
Lead bid defense presentations and contribute to study strategy development

Bachelor’s degree in Life Sciences or related field
5+ years in project management including +2 years Real-Word Evidence (RWE)
Strong knowledge of clinical study conduct, risk management and regulatory requirements
Therapeutic area expertise for Infectious Disease and/or Vaccines
Previous CRO experience required
Effective leadership, mentorship and management skills with attention to details
Demonstrates excellent analytical, organizational and problem-solving abilities
Proven ability to manage complex projects across geographies and functions
Proven ability to develop and manage timelines, tasks, milestones
Experience in vendor management and oversight
Experience managing and tracking study budgets and financials with participation and involvement with invoice and contract review and approvals
Excellent oral and written communication, presentation and interpersonal skills
Proficiency in MS Office and project management tools
ICH GCP awareness is a plus
Willingness to travel up to 20% as required

Senior Project Manager, RWE

Key skills