
1001 - 5000 employees
Founded 1989
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
Vertex Pharmaceuticals is a global biotechnology company focused on creating transformative medicines for people with serious diseases. With a commitment to scientific innovation, Vertex engages in the discovery, development, and production of cutting-edge therapies, particularly for conditions such as cystic fibrosis, sickle cell disease, and pain management. The company also emphasizes corporate responsibility and diversity within its inclusive culture to drive innovation and improve patient lives.
🔥 14 hours ago
🇺🇸 United States – Remote
💵 $80 - $85 / hour
⏳ Contract/Temporary
🟡 Mid-level
🟠 Senior
👷♀️ Project Manager
🦅 H1B Visa Sponsor
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1001 - 5000 employees
Founded 1989
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
Vertex Pharmaceuticals is a global biotechnology company focused on creating transformative medicines for people with serious diseases. With a commitment to scientific innovation, Vertex engages in the discovery, development, and production of cutting-edge therapies, particularly for conditions such as cystic fibrosis, sickle cell disease, and pain management. The company also emphasizes corporate responsibility and diversity within its inclusive culture to drive innovation and improve patient lives.
• Lead and coordinate global regulatory affairs advertising and promotion projects and portfolios • Align projects with organizational objectives, timelines, and corporate goals • Build and institutionalize regulatory project management frameworks, tools, and best practices • Provide strategic oversight of projects and portfolios • Coordinate communication among regulatory affairs, project teams, stakeholders, and external partners • Track project progress, materials, and deliverables • Identify and resolve issues proactively to maintain project momentum • Lead and participate in regulatory project meetings • Document meeting minutes, update project portals, and communicate outcomes to stakeholders • Perform administrative functions supporting project teams and department operations • Assume additional duties as assigned
• Bachelor’s degree in a scientific discipline, regulatory affairs, project management, or a related field • Minimum of 3 years’ experience in regulatory project management within the pharmaceutical or biotechnology industry, or an equivalent combination of education and experience • Experience managing cross-functional project teams • Ability to build project management frameworks, explain procedures, and drive regulatory advertising and promotion compliance initiatives • Excellent written and verbal communication skills, stakeholder engagement, briefing, and influencing skills • Strong organizational, analytical, and problem-solving skills • Proficiency in project and knowledge management software and techniques • Advanced computer skills with Microsoft platform, OneDrive, SharePoint, and regulatory platforms such as Veeva • Ability to work independently under moderate supervision and manage competing priorities across several projects • Familiarity with regulatory standards, guidelines, and submission requirements is preferred
• Overtime pay in accordance with federal and state requirements • Compensation, medical benefits, fringe benefits, and other employment terms presented by the third-party agency partner upon offer
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