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Kariusdx

Clinical Trial Associate

Kariusdx · Redwood City, CA (Hybrid) or Remote (USA)

Posted 27 days ago

or apply directly on Kariusdx's site. We never take the application ourselves.

Is this posting real?

This role has been open
27 days
Kariusdx's roles stay open a median of 23 days
Reposted
No
Salary listed
No
0% of Kariusdx's roles list one
Ghost-job risk at Kariusdx
low
0 stale, 0 reposted of 21 open
Hiring momentum
25 roles opened in the last 90 days
↑ up vs. the prior 90 days
Last confirmed on the employer's board
2026-09-17

Measured from postings appearing on and disappearing from Kariusdx's own lever board since 2026-08-04. Full hiring picture for Kariusdx.

About this role

The Clinical Trial Associate (CTA) at Karius supports clinical research activities by assisting with the collection, quality control, and quality assurance of regulatory documents related to clinical trials. The role involves maintaining the Trial Master File (TMF), communicating with study teams and clinical sites, and ensuring compliance with regulatory standards. The CTA will also help with study documentation, tracking milestones, and coordinating meetings, all while building proficiency in clinical trial processes under guidance.

Our read on this posting2.4out of 5
benefits
1/5
freshness
4/5
career value
3/5
role clarity
4/5
pay transparency
0/5

Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Kariusdx as an employer.

What you need

  • Bachelor's degree in life sciences, health sciences, clinical research, or a related field, or an equivalent combination of education and experience
  • 1-3 years of experience in clinical research, clinical operations, regulatory documentation, or a related environment
  • Basic understanding of clinical research processes and the role of study documentation in supporting compliant clinical trial execution
  • Familiarity with Trial Master Files (TMFs), Investigator Site Files (ISFs), or other clinical study documentation systems, or the ability to quickly learn applicable processes and standards
  • Basic knowledge of, or willingness to learn, ICH-GCP, FDA regulations, and other applicable clinical research requirements
  • Familiarity with medical and clinical research terminology, or demonstrated ability to learn technical terminology quickly

Nice to have

  • Exposure to clinical studies in infectious disease, microbiology, molecular diagnostics, genomics, or related life sciences
  • Familiarity with electronic Trial Master File (eTMF) platforms

Worth weighing

  • Remote work option available, but Bay Area preferred
  • Travel required up to 10-20%
  • Role involves significant documentation and administrative tasks, which may not appeal to all candidates

Summarised from Kariusdx's posting. Read the full original.

Listed by Kariusdx on their lever job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.

More roles at Kariusdx

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