Teams at ProPharma

Support statistical activities for clinical trials including study design, SAP development, and statistical analysis. Produce and ensure quality of statistical reports, tables, listings, and figures. Contribute to protocol and CRF review and develop/maintain SAS/R programs following SOPs, good programming practices, and regulatory guidelines.

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.