[Hiring] Clinical Services Project Manager I @Roche

Role Description

A healthier future. It’s 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. That’s what makes us Roche.

• Manages multiple clinical projects from initiation through completion, ensuring alignment with timelines, scope, and quality standards.
• Serves as the primary point of contact for Pharma and Roche clients, ensuring clear communication and stakeholder alignment.
• Coordinates project timelines and develops and executes project plans across CDx Pharma Services, aligning cross-functional activities and tracking progress against defined milestones.
• Identifies and mitigates risks, gaps, and bottlenecks, driving solutions to maintain project timelines.
• Oversees sample testing workflows and data reporting, ensuring accuracy, compliance, and adherence to quality standards.
• Collaborates with internal teams and external partners (e.g., CROs, investigators) to ensure seamless project delivery.
• Performs other duties as assigned by management.

Qualifications

• You hold a Bachelor’s Degree in Life Sciences, Clinical Research, Healthcare, or a related field, with a minimum of 2 years of experience in clinical project coordination and/or clinical trial management in a regulated environment OR
• You hold a Master’s Degree or have completed specialized training in Project Management or Clinical Research, and/or relevant certifications, with relevant experience supporting or managing clinical projects.

Requirements

• 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.
• Demonstrated ability to work under pressure while maintaining accuracy, data quality, and attention to detail.
• Proficiency with word processing, spreadsheet, database and email software (e.g., Microsoft Excel, Microsoft Word).
• Ability to collaborate cross-functionally, including interfacing with laboratory, scientific, and medical stakeholders.

Benefits

• Relocation Benefits are not offered for this job posting, this is a remote-based role.
• The expected salary range for this position based on the primary location of Arizona is 56,400.00 - 104,700.00 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.