Teams at ProPharma

Perform 3–6 veterinary GCP audits (1–2 days each) in Brazil or remotely. Audit sites against protocol, SOPs, local regulations, VICH GL9 and applicable GLP elements. Auditor schedules dates based on availability. One auditor per audit. Portuguese fluency required.

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 legal review and approval of promotional and non-promotional materials for pharmaceutical, biologic, device, and OTC products; provide strategic legal/regulatory guidance for PRC meetings and health authority interactions; ensure compliance with advertising/promotion regulations, support submissions to regulatory authorities, and collaborate with clients and teams to deliver high-quality work on time and within budget.