Jobs and Careers

Clinical Trial Manager #4179

Menlo Park, United Statesfull_timeVerifiedPosted 2 Apr 2025

💰 $138,000/yr($117,000/yr – $138,000/yr)

About the role

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 desiredAt 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 $