About The Position

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. Department Summary Assist in the coordination, and delivery of, moderate to complex Companions Diagnostic projects from Project Start through Product Launch. May support multiple projects across multiple product development phases. The Opportunity Manage tactical coordination, maintain detailed project plans, and track cross-functional progress to ensure all milestones are met on schedule and within budget. Partnering with Clinical Study Managers and CDMA teams to ensure strict adherence to GCP/GDP standards and the timely delivery of clinical data and reports. Lead the SARA process and utilize Salesforce to align departmental demand with staffing levels, ensuring resource security before contract execution. Organizing and leading project meetings, managing risk and action items, and overseeing interdepartmental activities to maximize resource efficiency. Implement industry best practices and foster internal knowledge sharing to drive process optimization and functional excellence. 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. 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.

Requirements

  • Education: Bachelor’s degree or a related technical field.
  • Experience: 3+ years of project management experience (or equivalent) in a highly regulated environment (Diagnostics, Pharma, or Biotech).

Nice To Haves

  • Certification: PMP or similar certification is a plus.

Responsibilities

  • Manage tactical coordination, maintain detailed project plans, and track cross-functional progress to ensure all milestones are met on schedule and within budget.
  • Partnering with Clinical Study Managers and CDMA teams to ensure strict adherence to GCP/GDP standards and the timely delivery of clinical data and reports.
  • Lead the SARA process and utilize Salesforce to align departmental demand with staffing levels, ensuring resource security before contract execution.
  • Organizing and leading project meetings, managing risk and action items, and overseeing interdepartmental activities to maximize resource efficiency.
  • Implement industry best practices and foster internal knowledge sharing to drive process optimization and functional excellence.

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Number of Employees

5,001-10,000 employees

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