Teams at ProPharma

Performs remote site monitoring and clinical trial support using centralized data and reporting tools. Supports study strategies, recruitment and enrollment tracking, drug supply and site payment reporting, data risk assessments, document collection, visit preparation, and study data review. Collaborates with clinical monitoring teams and study sites while following FDA regulations, ICH GCP, SOPs, and study plans.

Leads business development for Quality & Compliance Solutions in the life sciences sector. Builds client relationships, generates leads, manages sales opportunities, develops proposals, negotiates contracts, presents to prospects, attends industry events, and coordinates with marketing and client-facing teams to drive revenue and expand the client base.

Coordinates remote site activities for clinical research studies, serving as a point of contact for sites, supporting participant screening and recruitment, managing re-consenting and medical records, conducting protocol activities, entering and reviewing clinical data, responding to system queries, maintaining IRB/FDA-compliant documentation, and assisting with study closeout.