Teams at ProPharma

Lead analytical development for a synthetic team during a six-week contract. Develop HPLC methods supporting small-molecule API manufacturing and perform method qualification and validation, drawing on extensive pharmaceutical QC or analytical method development experience.

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.

Supports pharmaceutical quality systems by managing deviations, quality events, CAPAs, effectiveness checks, GxP change controls, audits, and regulatory inspections. Coordinates documentation, stakeholders, responses, and eQMS closure activities. Analyzes quality data and KPIs, prepares reports, investigates quality events, and evaluates medical information case and telephone quality. Requires strong organization, communication, attention to detail, and knowledge of GxP quality management systems.