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GRAIL is a healthcare company whose mission is to detect cancer early, when it can be cured.
The Role
The Clinical Trial Manager oversees clinical trial operations, ensuring regulatory compliance, managing sites, and collaborating across departments to improve efficiency and quality in trial execution.
Summary Generated by Built In
Our mission is to detect cancer early, when it can be cured. We are working to change the trajectory of cancer mortality and bring stakeholders together to adopt innovative, safe, and effective technologies that can transform cancer care.
We are a healthcare company, pioneering new technologies to advance early cancer detection. We have built a multi-disciplinary organization of scientists, engineers, and physicians and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicine’s greatest challenges.
GRAIL is headquartered in Menlo Park, California, with locations in Washington, D.C., North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies.
For more information, please visit grail.com.
The Clinical Trial Manager has overall responsibility to support Clinical Operations. This will include supporting overall day-to-day execution of a clinical trial, building strong internal and external relationships, managing clinical sites, and collaborating with cross functional teams.
This position will require a candidate to have experience with working in a fast paced environment, ability to work in ambiguity, proactive in seeking and utilizing the resources available to effectively problem solve, ability to be flexible and creative yet ensuring the clinical trial is executed within compliance of regulations and of the highest quality, and to be able to identify areas of improvement to drive efficiency within Clinical Operations.
Responsibilities:
- Manages all clinical operational aspects of a clinical trial from site selection, start-up, enrollment, maintenance, and close-out
- Prepares and reviews study related plans and documents including protocols, informed consent forms, recruitment plans, monitoring plans, protocol deviation plans, and case report forms with minimal supervision
- Participates in identifying, selecting, and monitoring the performance of clinical sites
- Ensures proper site training and management, provides ongoing oversight of clinical site compliance with study plans, study protocol, SOPs, FDA regulations, ICH/GCP guidelines, and in accordance with all applicable regulations
- Participates in EDC set-up by contributing to case report form design, user acceptance testing, completion guideline development and other related activities
- Identifies any potential risks to the study timelines and/or conduct, proposes mitigations and implements mitigations with cross-functional team and manager support
- Monitors clinical data entry progress and follows up on incomplete data entry and/or outstanding queries
- Contributes to the development and management of site budgets and ensures invoice payment according to site payment terms
- Works cross functionally with other departments such as Legal, Clinical Data Management, Biospecimen Management, Finance, Clinical Compliance, Clinical Development, and Lab Operations on all aspects of the clinical trial
- Provides oversight of regional study monitors and/or contract research organizations (CRO)Facilitate external communication with site staff and pharmaceutical partners (as applicable).
- Ensures Trial Master File (TMF) is current and maintainedProvides guidance and mentorship to CPAs (Clinical Project Assistants)
Preferred Qualifications:
- Bachelor’s degree or equivalent in the life sciences or related field required.
- Additional coursework in clinical trial planning and execution is strongly desired
- At least 5+ years of relevant experience in managing clinical trials at a sponsor company (pharma, biotech, or medical device) with a strong track record of successful trial initiation and execution
- Industry experience within in vitro diagnostics (IVD) highly preferred; pharmaceutical, biologics or medical device experience also acceptable
- Thorough knowledge of GCP, ICH guidelines and other US and international clinical regulatory requirements
- Working experience with an electronic data capture system, CTMS system, and eTMF system.
- Experience working on Investigational Device Exemption (IDE) and Real World Evidence (RWE) studies (highly preferred)
- Strong interpersonal communication (written and verbal), organizational and prioritization skills
- Able to work effectively under a fast-paced and changing environment
- Strong work ethic and demonstrated ability to deliver assignments on time
- Proficient with office automation tools, such as Microsoft Office and the Google suite of apps
The expected, full-time, annual base pay scale for this position is $117K - $138K for Menlo Park, CA. Actual base pay will consider skills, experience, and location.
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 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.
Top Skills
Ctms System
Electronic Data Capture System
Etmf System
Google Apps
MS Office
Next-Generation Sequencing
What the Team is Saying
Neda Ronaghi
Strategy and Operational Excellence Associate Director
Ruth Mauntz
Staff Bioinformatics Scientist
Tristan Matthews
Senior Director, Software Engineering
David Jenions
Principal Automation Engineer
Satnam Alag
SVP, Software Engineering
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The Company
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.
Typical time on-site:
2 days a week
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