Global Clinical Program Lead

🔥 8 hours ago

🌵 Arizona – Remote

🌵 Arizona – Remote

💵 $111.2k - $206.4k / year

⏰ Full Time

🟠 Senior

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Roche

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1896

🏥 Healthcare

⚕️ Healthcare Insurance

💊 Pharmaceuticals

Healthcare • Healthcare Insurance • Pharmaceuticals

Roche is at the forefront of technological advancements in healthcare. The company emphasizes the importance of diversity, equity, and inclusion across its global workforce of over 101,000 employees. Roche is particularly focused on research and development, digital innovation, and creating sustainable collaborations to benefit patients worldwide. With a strong culture of rewarding employee performance, Roche provides a diverse range of career opportunities in areas such as tech, manufacturing, and business strategy, encouraging innovation to transform global healthcare. The company also offers various programs for students and graduates, and operates in several countries, including Germany, Austria, and Switzerland.

📋 Description

• Drive the planning, development, and delivery of global evidence generation programs, maintaining accountability for program progress, budgets, timelines, and strategic risk management • Architect and lead Integrated Evidence Generation Plans (IEGP) for assigned products with internal and external stakeholders • Serve as strategic partner and primary interface between Clinical Development and Medical Affairs (CDMA) and Life Cycle Teams (LCTs) • Partner with Functional Partners and Sub-Chapter Leads to define resource requirements and coordinate capacity across CDMA Networks and Project Teams • Oversee program-level budgets and trial timelines, performing proactive scenario assessments to mitigate operational and regulatory risks • Align Regulatory Affairs, R&D, Diagnostics Partners, and cross-functional CDMA chapters for seamless trial execution • Champion a patient- and customer-centric mindset across global matrixed teams

🎯 Requirements

• Bachelor’s degree in a scientific discipline or related field • 8+ years of project or clinical trial coordination/management experience within a regulated CRO, diagnostic, or pharmaceutical environment • Proven track record managing clinical trial execution, bio-sample testing/management, and quality assurance processes under strict timelines • Demonstrated ability to lead by influence and drive consensus within a heavily matrixed, multi-site global organization • Deep mastery of international regulatory standards (ICH-GCP, ISO, GMP, GLP) and diagnostic/medical testing environments (FDA, CAP, CLIA, WHO) • Ability to travel approximately 20% (Domestic and International)

🏖️ Benefits

• A discretionary annual bonus may be available based on individual and Company performance • Benefits detailed at the link provided below • Remote work may be considered based on the candidate's experience and location