Note: The job is a remote job and is open to candidates in USA. 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
Skills
- 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
Benefits
- A discretionary annual bonus may be available based on individual and Company performance.
- This is a remote based role.
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