Clinical Program Leader
Location: Tucson, Arizona, United States of America
Job Category: Research & Development (Clinical Trials / Clinical Program Management)
Job ID: 202602-102734
Experience Required: 10+ years in clinical trials within Diagnostics, Biotech, or Pharmaceutical industries
Company Overview
Roche is a global leader in pharmaceuticals and diagnostics, committed to improving patient outcomes through innovation and scientific excellence. With over 100,000 employees worldwide, Roche drives advancements in healthcare, enabling access to life-changing treatments and diagnostics. The company fosters an inclusive culture where individual contributions are valued, ideas are encouraged, and professional growth is supported.
Position Overview
The Clinical Program Leader will serve as a strategic leader within the Clinical Development & Medical Affairs (CDMA) function. This role provides oversight and direction for global evidence generation programs, ensuring that clinical trials and diagnostic solutions are supported by robust data to improve patient outcomes. Reporting into Life Cycle Teams (LCTs), the Clinical Program Leader will lead complex, multi-national clinical trials from planning to regulatory submission.
Key Responsibilities
Strategic Leadership: Align clinical strategies with LCTs, Project Teams, and CDMA objectives to support evidence generation and patient-focused outcomes.
Evidence Generation: Lead the planning and execution of registrational and non-registrational clinical trials, ensuring accountability for timelines, budgets, and quality deliverables.
Matrix Influence: Collaborate with Regulatory Affairs, R&D, Diagnostics Partners, and CDMA chapters to assess risks and implement proactive strategies.
Functional Partnership: Serve as the primary advisor for LCTs, managing resources, priorities, and program budgets.
Integrated Planning: Develop and implement Integrated Evidence Generation Plans (IEGPs) in consultation with internal stakeholders and external Key Opinion Leaders (KOLs).
Resource & Financial Oversight: Oversee program-level budgets, resource allocation, and alignment with Sub-Chapter Leads.
Operational Excellence: Ensure all trial activities comply with Design Control requirements, SOPs, and international regulations (FDA, CE-Mark, IVD).
Documentation & Technical Expertise: Provide guidance for trial protocols, monitoring plans, clinical study reports (CSRs), and ensure high-quality trial conduct.
Qualifications & Experience
Bachelor’s degree in a scientific discipline (advanced degree preferred).
Minimum of 10 years of progressive experience in clinical trial management within Diagnostics, Biotech, or Pharmaceutical industries.
Proven ability to lead cross-functional teams in a global, matrixed organization.
Strong knowledge of international regulatory standards (ICH-GCP, ISO, GMP, GLP) and clinical testing environments (FDA, CAP, CLIA, WHO).
Experience managing complex multi-million dollar program budgets and strategic planning.
Ability to travel up to 20% internationally and domestically.
Locations: Tucson, AZ | Penzberg, Germany | United Kingdom
Compensation & Benefits
Tucson, AZ Salary Range: $127,500 – $236,700 USD per annum (actual pay based on experience, qualifications, and geographic location).
Discretionary annual bonus.
Roche Long Term Incentive Plan (LTIP).
Comprehensive medical, dental, and vision insurance.
401(k) with company matching and paid time off.
Why Join Roche
Joining Roche offers the opportunity to work on cutting-edge clinical development programs, influence global healthcare outcomes, and collaborate with a diverse, innovative team dedicated to scientific excellence. Roche is committed to equality, inclusion, and transparent pay practices.
Apply Today
If you are an experienced clinical leader ready to drive evidence-based patient solutions in a global organization, Roche invites you to apply.
Equal Opportunity Employer
Roche provides equal employment opportunities to all employees and applicants without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, veteran status, or other legally protected characteristics. Accommodations are available for applicants with disabilities during the application process.
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