Clinical Services Project Manager I

Roche•Tucson, AZ
•$56,400 - $104,700•Remote

About The Position

At Roche, the culture encourages personal expression, open dialogue, and genuine connections, with the goal of helping employees thrive personally and professionally while advancing access to healthcare. The Clinical Project Manager manages clinical projects from initiation through completion as part of a remote team. The role aligns cross-functional activities, mitigates risks, and drives solutions to maintain quality standards and deliver projects successfully. The expected annual salary range for the primary location of Arizona is $56,400 to $104,700 USD. Actual pay depends 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. Relocation benefits are not offered.

Requirements

  • Bachelor’s degree in Life Sciences, Clinical Research, Healthcare, or a related field, and a minimum of 2 years of experience in clinical project coordination and/or clinical trial management in a regulated environment; alternatively, a Master’s degree or specialized training in Project Management or Clinical Research and/or relevant certifications, with relevant experience supporting or managing clinical projects.
  • Strong problem-solving, organization, and project coordination skills, with the ability to manage timelines and milestone-driven deliverables.
  • Solid understanding of clinical trials, regulatory and quality processes, including clinical sample and laboratory workflows.
  • Effective communication and interpersonal skills, with the ability to collaborate across teams and facilitate meetings.
  • Ability to work under pressure while maintaining accuracy, data quality, and attention to detail.
  • Proficiency with word processing, spreadsheet, database, and email software, such as Microsoft Excel and Microsoft Word.
  • Ability to collaborate cross-functionally, including interfacing with laboratory, scientific, and medical stakeholders.

Responsibilities

  • Manage multiple clinical projects from initiation through completion, ensuring alignment with timelines, scope, and quality standards.
  • Serve as the primary point of contact for Pharma and Roche clients, ensuring clear communication and stakeholder alignment.
  • Coordinate project timelines and develop and execute project plans across CDx Pharma Services, aligning cross-functional activities and tracking progress against defined milestones.
  • Identify and mitigate risks, gaps, and bottlenecks, driving solutions to maintain project timelines.
  • Oversee sample testing workflows and data reporting, ensuring accuracy, compliance, and adherence to quality standards.
  • Collaborate with internal teams and external partners, such as CROs and investigators, to ensure seamless project delivery.
  • Perform other duties as assigned by management.

Benefits

  • A discretionary annual bonus may be available based on individual and Company performance.
  • Benefits are referenced via a link in the posting, but specific benefits are not listed.
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service