Jobs at ProPharma

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.

The Product Complaint Specialist evaluates product complaint cases, coordinates follow-ups, manages correspondence, and provides administrative support, ensuring adherence to regulatory standards.

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.