GRAIL is a healthcare company whose mission is to detect cancer early, when it can be cured. GRAIL is focused on alleviating the global burden of cancer by developing pioneering technology to detect and identify multiple deadly cancer types early. The company is using the power of next-generation 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 its multi-cancer early detection blood test. GRAIL is headquartered in Menlo Park, CA with locations in Washington, D.C., North Carolina, and the United Kingdom. GRAIL, LLC is a wholly-owned subsidiary of Illumina, Inc. (NASDAQ:ILMN). For more information, please visit www.grail.com.
GRAIL is currently looking for Program Management expertise and support our teams working in the Laboratory Operations function. The successful candidate will be comfortable working on projects across, but not limited to, various operations-related functional areas including Engineering Operations, MSAT, Lab Operations, Technical Operations, Study Management, and key partner functions including Quality.
In this role you will be responsible for ensuring all project milestones and deliverables are met, and that activities are well executed and managed. Responsibilities include the day-to-day planning, coordinating, and tracking of critical activities including management of cross-
functional projects interfacing with the functional groups listed above (amongst others), as well as with subject matter experts at GRAILβs laboratory facilities. GRAIL's successful candidate will partner with functional and Life Cycle team leaders to optimize teamsβ effectiveness, decision-making, and communication and utilize robust negotiating skills to facilitate integrated decision-making for laboratory operations.
Responsibilities:
β Create and drive timelines to keep project(s) on schedule.
β Establish and maintain functionally integrated project schedules.
β Utilize tracking tools to enable effective project management across various functional areas.
β Schedule, organize, and drive project team meeting(s): prepare and distribute agendas/minutes;
track action items, and escalate areas of risk to the appropriate management entity.
β Facilitate communication of issues and outcomes to the Core Team/Project team leadership.
β Manage the interfaces between functional areas and ensure effective handoff and
communication between department functions to execute on important project milestones.
β Works with project leaders and/or SMEβs to prepare status reports, specific project updates, or
scenarios.
β Manage document review processes to support functional activities and other key project
deliverables.
β Engage with quality and regulatory functions to ensure operational planning and execution meets
expected standards.
β Collaborate with site Leadership/teams to define project-related budget assumptions for the
annual operating plan.
β Project manage cross-functional investigations interfacing with groups across the organization.
Qualifications:
This job requires a combination of analytical, organizational, and interpersonal skills. The ideal candidate will have a blend of project management and laboratory operations knowledge in the medical diagnostics industry. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability
required. Reasonable accommodations may be made to enable individuals with disabilities to perform the
essential functions.
Requirements:
β Minimum of a BA/BS is required with 5-8 years of experience, Masters with 2-5 years of related
experience, or PhD with 0-2 years of related multidisciplinary experience in the device/diagnostic/biotech/pharmaceutical industry, with 1-5 years of direct project management experience in laboratory operations or a supporting function e.g. technical operations, MSAT,
Engineering Operations, clinical laboratory operations.
β Experience working under design control and design transfer from development to commercial
operations is highly desirable.
β Experience working with regulatory on post approval changes is highly desirable.
β Experience with global sample and lab operations is highly desirable.
Key Attributes for a successful candidate:
β Proactive/not passive: Motivated to solve problems and create/manage situations to move
forward while keeping the whole team intact through positive energy.
β Communication: Can distill complex scenarios/ideas into clear messages and next steps to a
broad audience
β Adaptive: Can pivot quickly to new ideas, direction and process while being grounded in defining
what success looks like.
β Resilient: Comfortable in tough situations, can be relied on in tense circumstances, and will face
difficult challenges with poise and self-assurance. For example, comfortable influencing decision-
making of others internally, across functions/team, and at any level.
Based on the role, colleagues may be eligible to participate in an annual bonus plan tied to company and individual performance, or an incentive plan. We also offer a long-term incentive plan to align company and colleague success over time.
In addition, GRAIL offers a progressive benefit package, including flexible time-off, a 401k with a company match, and alongside our medical, dental, vision plans, carefully selected mindfulness offerings.
GRAIL is an Equal Employment Office and Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. We will reasonably accommodate all individuals with disabilities so that they can participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. GRAIL maintains a drug-free workplace.