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ProPharma is seeking a Clinical Project Manager to lead studies from start to closeout, coordinating timelines, budgets, and cross‑functional teams across regulatory sciences, clinical research solutions, quality, and pharmacovigilance. You will ensure FDA/ICH-GCP compliance and clear communication with sponsors and stakeholders.
Responsibilities include risk assessment, change orders, TMF oversight, vendor coordination, and performance metrics.
ProPharma is seeking a Clinical Project Manager to lead studies from start to closeout, coordinating timelines, budgets, and cross‑functional teams across regulatory sciences, clinical research solutions, quality, and pharmacovigilance. You will ensure FDA/ICH-GCP compliance and clear communication with sponsors and stakeholders.
Responsibilities include risk assessment, change orders, TMF oversight, vendor coordination, and performance metrics.