Clinical Trial Assistant
The Clinical Trial Assistant supports oncology clinical trial execution by managing study documents, maintaining trial master files, and coordinating meetings. This role requires collaboration with cross-functional teams and CRO partners to facilitate clinical operations, ensuring smooth study startup, maintenance, and closeout activities.
About Careertakes
👉 Important disclosure: Careertakes is a third-party recruiting platform supporting this hiring process. If selected, you will be employed directly by our client, Scientific & QA.
Applicants for this role may also receive access to additional matched opportunities through the Careertakes platform.
What You’ll Do
Confidential Client is seeking an entry-level Clinical Trial Assistant to support oncology clinical trial execution and clinical operations. This is a hands-on role that supports study documentation, trial master file maintenance, meeting coordination, and communication with internal teams and CRO partners.
- Develop, review, archive, and maintain study-specific documents, training materials, and manuals
- Establish and maintain Trial Master Files (TMFs) and coordinate TMF activities with CRO partners
- Create, update, and track information for key study activities in clinical systems
- Prepare meeting materials, schedule meetings, and capture meeting minutes and action items
- Collect investigator and site information for study startup, maintenance, and closeout
- Support cross‑functional clinical operations tasks as assigned
Qualifications
- RN or Bachelor’s degree in biological sciences, nursing, or related health/science field
- 1–3 years of relevant experience in pharmaceutical, biotech, or clinical research support roles
- Proficiency with Microsoft Word, Excel, and PowerPoint
- Strong written and verbal communication skills
- Able to multitask, prioritize, and work in a fast-paced, cross-functional environment
- Willingness to travel approximately 25% of the time
Location & Travel
- Onsite or hybrid role based in Portola Valley, CA (work location per authoritative listing).
- Travel: Approximately 25% for site startup, monitoring support, or meetings.
Why Apply (Recruiter Note)
As a third‑party recruiter, Careertakes works with Confidential Client to present this opportunity for candidates who want early-career growth in clinical operations and hands-on exposure to oncology trials. This role is a strong fit if you want to build skills in Trial Master File management, CRO coordination, and cross-functional clinical study support.
- Estimated salary (job-board estimate): $87,947 per year — provided for transparency; final compensation determined by Confidential Client.
- Entry-level / early-career growth path into clinical operations and clinical research.
Equal Opportunity & Hiring Transparency
Careertakes and our client are Equal Opportunity Employers committed to building a diverse and inclusive workforce. We prohibit discrimination or harassment of any kind.
To support a fair and efficient hiring process, AI tools may be used to assist with application review or resume screening. These tools do not replace human decision-making. Final hiring decisions are made by people.
If you have questions about how your data is used, please contact us directly.
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