Global Clinical Program Lead

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim to prevent stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche where every voice matters.

A healthier future. Its what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. Thats what makes us Roche.

The Opportunity:

• You will ensure proactive alignment with LCT (Life Cycle Teams) / PT (Project Teams) medical/clinical evidence generation and execution strategies within CDMA.
• You will drive planning development and delivery of evidence generation programs with full accountability for the program progress budgets timelines strategic scenario assessments and proactive program risk management in partnership with cross-functional stakeholders including LCT Project Leads Regulatory Affairs R&D (Research & Development) Pharma 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.
• Ensure adequate allocation of resources by collaborating with the Functional Partner (FP) and Sub-Chapter Leads (SCL) through timely communication of demands and skill set requirements in alignment with priorities of the respective CDMA Networks and Project Teams.

Who You Are:

• You have a Bachelors degree or an advanced degree in Life Sciences and/or relevant expertise in the healthcare industry a related field or equivalent relevant experience. Experience in diabetes care is a must background in multiple disease areas is a plus.
• Generally 10 years of experience in diagnostics medical device biotechnology and/or pharmaceutical clinical trials with responsibilities for managing all major aspects of strategic planning design organization implementation and delivery of clinical programs.
• Understands applies good knowledge of and ensures adherence to ICH-GCP IVDD/IVDR MDR SaMD FDA Bfarm NMPA regulations etc across the respective programs to ensure objectives are met in support of CDMA and/or Diagnostics goals.
• You are able and willing to travel up to 25% (can vary/month/program)

Knowledge Skills and Abilities

• 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 Roches values of integrity courage and passion and Diagnostics (culture mindset and behaviors) in everything you do.

Relocation benefits are not available for this job posting.

The expected salary range for this position based on the primary location of Pleasanton CA is $146600 - 272200 USD Annual. Actual pay will be determined based on experience qualifications geographic location and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.

This position also qualifies for the benefits detailed at the link provided below. Benefits

A healthier future drives us to innovate. Together more than 100000 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.

Lets 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 companys 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.

If you have a disability and need an accommodation in relation to the online application process please contact us by completing this form Accommodations for Applicants.