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Tier-1 brand, metro location, and common project manager title increase applicant density.
Role requires domain-specific clinical research and regulatory knowledge, so background transferability is low.
Explicit 6+ years, required clinical trial expertise and regulatory compliance increase filtering strictness.
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Manage end-to-end operational activities for all Externally Sponsored Research (ESR) studies from proposal submission through study closeout, ensuring compliance with SOPs and regulatory requirements.
Coordinate cross-functional teams for timely delivery of research agreements, supply management, contracting, regulatory documentation, and payments tracking within ESR programs.
Develop and maintain project timelines, reporting metrics and KPIs, support audit readiness, and oversee ESR system integrity and stakeholder training.
6+ years of experience in Clinical Research & Development including clinical trial project management.
Degree in Medical, Pharmaceutical, scientific, or related Life Sciences discipline with substantial project management or clinical trials experience.
Knowledge of Medical Investigator Sponsored Studies program requirements and regulatory environment including GCP, ICH, OIG, PhRMA code preferred.
Project management certification preferred; Travel as per business needs.
Experienced in collaborating cross-functionally with R&D, supply, and regulatory teams to drive efficient and compliant clinical study execution.
Comfortable managing complex projects involving multiple stakeholders and systems with strong analytical and process improvement focus.
Demonstrates capability in producing and analyzing performance metrics and KPI reports to inform strategic investment and operational decisions.