Teams at ProPharma

Lead and manage client-facing pharmacovigilance projects including timelines, risk and change control, KPIs, financials, audits, cross-functional coordination, training, and client communications to ensure compliance and delivery of PV project objectives.

Conduct statistical analyses and support clinical trial design, sample size calculations, randomization, and SDTM/ADaM data preparation. Develop and QC statistical analysis plans, programs, TLFs, and analysis datasets with senior oversight. Participate in unblinding, review CSRs for accuracy, attend project meetings, and interact with clients while maintaining documentation and compliance.

Lead statistical activities for clinical trials including study design, SAP development, statistical analysis, and deliverables (tables, listings, graphs). Program in SAS/R, ensure regulatory compliance and CDISC standards, mentor junior statisticians, and support cross-functional teams.