at Grail
Location
Menlo Park, CA
Compensation
$69k–$81k USD
Type
full time
Posted
6 days ago
Remote
Yes
Market range · function + seniority
p25 · target · p75 · n=115
Posted $81k · well below market
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The Clinical Project Assistant has overall responsibility to support the study teams within Clinical Operations. This will include supporting administrative aspects of clinical trial execution and working under general supervision for routine tasks and with detailed instructions.
This position will require a candidate to have a good overall understanding of the major areas within clinical operations.
This role is based in Menlo Park, California, and will move to Sunnyvale, California in Fall 2026. It offers a flexible work arrangement, with the ability to work from GRAIL's office or from home. Our current flexible work arrangement policy requires that a minimum of 40%, or 16 hours, of your total work week be on-site. Your specific schedule, determined in collaboration with your manager, will align with team and business needs and could exceed the 40% requirement for the site. At our Menlo Park campus, Tuesdays and Thursdays are the key days where we encourage on-site presence to engage in events and on-site activities.
Maintain and perform periodic review of the Trial Master File (TMF) for completeness and accuracy
Track site payments and vendor invoices
Assist study team in tracking and reporting on key study quality metrics and in determining appropriate action in conjunction with study team
Support development of relevant tracking tools and other internal processes to increase departmental efficiency
Participating in continuous improvement initiatives
Assist with meeting coordination, meeting materials and meeting minutes.
Support other job-related duties as assigned by the Clinical Lead or designee
Bachelor’s degree in a related scientific discipline
At least 1 year of relevant experience in the pharmaceutical/biotech/medical device industry
Working knowledge of GCPs, Trial Master Files, ICH guidelines or experience working in a regulated environment
Working experience with an electronic trial master file (eTMF) system and strong database skills
Strong work ethic and demonstrated ability to deliver assignments on time
Attention to details and organizational skills
Ability to coordinate and prioritize multiple tasks
Good problem-solving skills
Strong communication skills
Positive, self-starter, flexible; ability to adapt to changing priorities
Ability to establish and maintain effective working relationships in a team environment
Ability to work collaboratively in a dynamic and fast paced environment