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Open nowPosted 2 days ago

Clinical Research Associate – IL Student Position (Part-Time)

Ibex Medical Analytics5 open roles

Where
Tel aviv, HaMerkaz, Israel
Work mode
Hybrid
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Your applicationOpen nowClinical Research Associate – IL Student Position (Part-Time)Ibex Medical Analytics · Tel aviv, HaMerkaz, Israel

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The clock on this job

Early applications get read.

9.0% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 1.8%1 day
  2. 3.9%3 days
  3. 9.0%7 days
  4. 15.5%14 days
  5. 34.1%30 days
This job: posted 2 days ago

The posting

  • Provide operational and scientific support for global clinical validation and research studies under the guidance of the Director of Clinical & Scientific Affairs. Key responsibilities include supporting protocol development, study reports, scientific conference deliverables (posters and presentations), and regulatory documentation while collaborating cross-functionally to ensure rigorous and timely study execution.
  • Proactively contributes to clinical study processes by supporting the execution and tracking of clinical operations, ensuring compliance with company SOPs, ICH-GCP guidelines, regulatory requirements, and patient safety standards.
  • Assists in developing and writing clinical study protocols, study plans, Ethics/IRB submission packages, CRFs, and clinical study reports.
  • Facilitates training for clinical study teams according to study protocols and maintains strong relationships with investigators and external experts to support effective project delivery.
  • Supports data quality initiatives and helps implement activities required for timely, high-quality deliverables (e.g., collaborating with statisticians and data managers, participating in data review).
  • Analyzes, interprets, and presents clinical study results to internal and external stakeholders, including contributing to scientific peer-reviewed publications.
  • Graduate student in the advanced stages of PhD (optional MD) in Life Sciences, Biomedical Engineering, or a related discipline.
  • Previous experience in conducting medical device or IVD clinical studies – Significant advantage.
  • Knowledge of oncology, pathology, medical device/IVD clinical development, and a deep understanding of molecular pathways and biopharma development in oncology - Preferred.
  • Experience contributing to research planning, study design, clinical operations, data handling, biostatistics, scientific posters, presentations, and manuscript drafting.
  • Demonstrated ability to work both independently and collaboratively to execute complex study plans, protocols, methodologies, and study timelines under general guidance.
  • Solid understanding of the clinical operations value chain, with a proven track record of supporting study planning, execution, data management, and clinical study reporting

*We are an equal opportunity employer and committed to creating a friendly, inclusive environment that is a pleasure to work in, and where there is an unbiased acceptance of others.

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