Jobs 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.

Lead statistical design and analysis for clinical trials, develop analysis plans and SAS/R programs, ensure quality of tables/reports/figures, advise cross-functional teams, maintain regulatory compliance and internal SOPs, and mentor junior statisticians.

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

The Product Integrity Specialist reviews product complaints and adverse events, conducts follow-up calls, manages reports, and provides administrative support.