Global Clinical Program Lead, Diabetes Evidence & Delivery

Roche

Pleasanton (CA)

On-site

USD 147,000 - 272,000

Full time

6 days ago

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Job summary

Roche in Pleasanton, CA is seeking an experienced leader to drive planning, development, and delivery of evidence generation programs across CDMA. You will manage budgets, timelines, and risks while partnering with Regulatory Affairs, R&D, and Pharma Partners to advance diagnostics and SaMD initiatives.

The role requires 10+ years in diagnostics/biotech/pharma clinical trials, a Life Sciences degree, and travel up to 25%.

Qualifications

Drive patient and customer-centricity by always putting patients and the customers first.
Partner across diverse regions, cultures, and time zones to create an environment of belonging, inclusion and diversity.
Work across Clinical Development and Medical Affairs 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 We@Roche Diagnostics in everything you do.

Responsibilities

Drive planning, development, and delivery of evidence generation programs with full accountability for program progress, budgets, timelines, strategic scenario assessments, and proactive program risk management in partnership with cross-functional stakeholders.
Drive the development of the Integrated Evidence Generation Plan for the products in scope in partnership with internal and external stakeholders.
Ensure adequate allocation of resources by collaborating with the Functional Partner and Sub-Chapter Leads, through timely communication of demands and skill set requirements.
Align with priorities of the respective CDMA Networks and Project Teams.