Back
Tier‑1 employer, metro role and generalist PMO skillset drive high candidate competition.
Requires pharma/regulatory experience and RWE/domain knowledge, so industry background heavily influences fit.
Explicit 7+ years, pharma/regulatory experience requirement and mandatory tool/compliance skills create high shortlisting strictness.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Oversee execution of CfOR operational projects and global observational research studies ensuring timely delivery within budget, quality, and compliance standards.
Drive process optimization and AI-enabled operational transformation across budgeting, compliance, contract management, and reporting workflows.
Manage project planning, governance tracking, milestone management, risk/issue tracking, and stakeholder reporting using tools like SharePoint and Smartsheet.
Bachelor’s degree with 7+ years scientific or operations experience OR Master’s degree with 5+ years scientific or operations experience.
Minimum 5 years project management experience including 3+ years in pharma/biotech and cross-functional settings.
Strong experience with budgeting, vendor management, regulated document management systems, and compliance with GCP, FDA, and regulatory frameworks.
Proficiency with digital and collaboration tools such as AI platforms (ChatGPT/Copilot), Smartsheet, SharePoint, MS Teams, and dashboard/reporting software (Power BI, Excel).
Experience operating within pharma/biotech environment with knowledge of drug commercialization and clinical operations regulatory compliance.
Skilled in applying project management office (PMO) practices including Agile/Scrum/Kanban to improve operational efficiency and execution visibility.
Strategic operator with strong analytical skills and demonstrated ability to lead digital transformation and automation initiatives in a regulated scientific operations setting.