Teams at ProPharma

Oversee and perform daily adverse event case processing for clinical trial and post-market ICSRs, including MedDRA coding, seriousness/expectedness assessment, follow-up, narrative writing, client notifications, peer review, HCP review, training, mentoring, and PV subject-matter oversight to ensure global safety compliance and quality.

Coordinate day-to-day site communications and document submissions for clinical studies. Support screening, recruitment, re-consenting, medical record collection, protocol activities, data entry, query resolution, maintain IRB/FDA-compliant documentation, assist with closeout, and perform other study-related tasks as directed.

Support project managers by developing plans, coordinating activities, scheduling meetings, tracking progress, monitoring risks and issues, preparing reports and budgets, maintaining project documentation, and providing administrative support to ensure projects are delivered on time, within scope, and within budget.