Clinical Services Project Manager I

Roche is a healthcare and diagnostics company focused on advancing science and improving access to healthcare. The Clinical Services Project Manager I will manage clinical projects from initiation through completion, coordinating cross-functional activities, timelines, risks, sample testing workflows, and data reporting while maintaining quality and compliance standards.

Responsibilities:

• 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

Requirements:

• 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
• 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
• This is a remote based role