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As a Clinical Program Lead within the Clinical Development and Medical Affairs (CDMA) chapter, you provide high-level strategic leadership and scientific rigor for global evidence generation programs. You act as the primary strategic architect between Life Cycle Teams (LCT) and clinical execution, ensuring diagnostic solutions are backed by robust data to improve patient outcomes.
Operating as a senior leader in a matrixed environment, you drive the development of Integrated Evidence Generation Plans (IEGP) and oversee the delivery of complex global clinical trials from inception through to regulatory success.
Key Accountabilities
The key accountabilities for this position include, but are not limited to:
Ensure proactive alignment with LCT (Life Cycle Teams) / PT (Project Teams), medical/clinical, evidence generation and execution strategies within CDMA.
Drive planning, development and delivery of evidence generation programs with full accountability for the program progress, budgets, timelines, strategic scenario assessments, proactive program risk management in partnership with cross-functional stakeholders including LCT Project Leads, Regulatory Affairs, R&D (Research & Development), Diagnostics Partners and other CDMA chapters.
Drive the development of the Integrated Evidence Generation Plan for the products in scope in partnership with internal and external stakeholders.
In collaboration with the Functional Partner (FP) and Sub-Chapter Leads (SCL), ensure adequate allocation of resources by timely communication of demands and skill set requirements in alignment with priorities of the respective CDMA Networks and Project Teams.
May be nominated as Functional Partner acting as the key strategic partner for LCTs (primary interface of CDMA and LCTs) with subject matter expertise, providing guidance for priority, budgets and capacity coordination within chapter and/or sub-chapter; enabling the joint CDMA delivery on the LCT strategy and collaborating with CDMA Network, Indication Leads and CDMA Chapters to align strategic decisions at the CA LT (Customer Areas Leadership Teams) and SPC (Solution Portfolio Committee).
Accountable for the oversight of program-level budget of assigned programs.
Responsibilities
The following are responsibilities for the individuals in this position:
Drive patient and customer-centricity (mindset, behaviors and actions) by always putting the needs of patients and the customers first.
Partner across diverse regions, cultures, and time zones to create an environment of belonging, inclusion and diversity.
Working across Clinical Development and Medical Affairs communities to identify mutual value and opportunities for collaboration.
Demonstrate flexibility and adaptability to perform in a fast-paced, matrixed environment where fluid, cross-team collaboration is crucial.
Leverage excellent verbal and written communication skills (English).
Model Roche’s values of integrity, courage, and passion and operating principles (culture, mindset and behaviors) in everything you do.
Education: Bachelor’s degree in a scientific discipline or related field (Advanced degree preferred).
Experience: 10+ years of progressive experience in clinical trials within the Diagnostics, Biotech, or Pharmaceutical industries.
Senior Leadership: Proven ability to lead by influence in a heavily matrixed, multi-site global organization; experience interacting with executive management.
Regulatory Mastery: Deep knowledge of international standards (ICH-GCP, ISO, GMP, GLP) and medical testing environments (FDA, CAP, CLIA, WHO).
Strategic Agility: Highly autonomous with the ability to initiate change, manage complex multi-million dollar budgets, and drive results through external resources.
Locations: Tucson, AZ | Penzberg, Germany | UK
Local candidates are preferred, but remote work may be considered based on the candidate's experience and location.
Travel: Ability to travel approximately 20% (Domestic and International).
Tucson, AZ Salary Range: $133,400.00 - $247,700.00 USD Annual Annual Actual pay will be determined based on experience, qualifications, and other job-related factors permitted by law.
Roche Benefits Include:
Discretionary Annual Bonus based on performance.
Roche Long Term Incentive Plan (LTIP).
Comprehensive Medical, Dental, and Vision insurance.
401(k) with company matching and paid time off.
Global Grade: SE8
Please note that the global grade displayed is a target global grade for the role and the actual global grade offered to a candidate may vary depending on several factors - including scope and breadth of the role. For further information relating to global grading in Roche please visit the global grading gSite.
Roche is dedicated to ensuring fair and transparent pay practices for its employees. In compliance with state legal requirements, you may notice some of our job postings will now list salary ranges. Please note that the broad ranges are aligned with our global grading framework and, in some cases, may also include geographic differentials.
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Roche is an equal opportunity employer.
Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Tucson. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let’s build a healthier future, together.
Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
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