Responsibilities
- Lead the planning, execution, and governance of large-scale programs with moderate to high complexity and strategic importance.
- Partner with cross-functional teams to ensure integrated program plans are aligned with corporate objectives and product lifecycle goals.
- Monitor and control project scope, timelines, risks, and interdependencies to ensure successful delivery of key milestones and deliverables.
- Facilitate communication and alignment across Development, Research, and Operations to optimize cross-functional collaboration and decision-making.
- Apply expert-level knowledge of project management principles, design controls, and regulatory frameworks to ensure compliant execution of product development activities.
- Act as a GDO Program Management subject matter expert (SME) by contributing to best practices, process improvements, and tool development within the organization.
- Oversee and manage program-level schedules, budgets, resource plans, and performance metrics.
- Prepare and deliver program updates, risk assessments, and mitigation plans to stakeholders and executive leadership.
- Support cross-functional investigations and process improvements aimed at enhancing operational readiness and execution quality.
- Collaborate with quality and regulatory partners to ensure alignment with internal standards and external regulatory expectations.
- Contribute to long-range strategic planning for the Development portfolio, including budgeting and capacity forecasting.
Preferred Qualifications
- Bachelor’s degree in a scientific, engineering, or technical discipline and 8–12 years of relevant experience; or Master’s degree with 5–8 years; or PhD with 2–5 years in the diagnostics, medical device, pharmaceutical, or biotech industry.
- 2+ years of direct program or project management experience in regulated product development or clinical laboratory operations.
- Demonstrated experience working under design control and executing design transfer processes.
- Familiarity with managing post-approval regulatory changes and associated cross-functional impacts.
- PMP Certification is highly desirable.
- Ability to travel 10-20%.
- Strategic thinker with strong analytical and problem-solving capabilities.
- Proficient in program management tools and methodologies (e.g., MS Project, Smartsheet, JIRA, Workday Project, or equivalent).
- Effective communicator with the ability to engage and influence stakeholders at all organizational levels.
- Demonstrated ability to operate independently, exercise sound judgment, and drive initiatives to completion.
- Proven track record in navigating complex, matrixed environments and leading cross-functional teams.
Similar Jobs
What We Do
GRAIL is a healthcare company whose mission is to detect cancer early, when it can be cured. GRAIL is using the power of high-intensity sequencing, population-scale clinical studies, and state-of-the-art computer science and data science to enhance the scientific understanding of cancer biology, and to develop and commercialize pioneering products
Why Work With Us
Everything we do is guided by our mission to detect cancer early, when it can be cured. It’s the reason we’re here, and it’s no small task.
The right people make all the difference. That’s why we’re looking for those who strive to share their knowledge, contribute their skills, inspire each other and commit to something bigger than themselves.
Gallery










GRAIL Offices
Hybrid Workspace
Employees engage in a combination of remote and on-site work.
GRAIL has a variety of work types depending on the roles. Some are onsite like a lab role, others are hybrid and still others are remote. Hybrid is typically Tuesday and Thursday but leaders may be flexible depending on the role.