Clinical Research Coordinator – Oncology (On‑site, Full‑time)
Soroka Medical Center · Beer-Sheva
Job description
About the role
The Clinical Research Coordinator will support oncology studies by ensuring that all research activities are conducted in compliance with Good Clinical Practice (GCP) and regulatory requirements. Working under the principal investigator, the coordinator will manage patient enrollment, documentation, and data integrity throughout the study lifecycle.
Key responsibilities
- Assist in recruiting and enrolling eligible oncology patients.
- Coordinate, monitor, and document all study‑related activities according to GCP protocols.
- Maintain up‑to‑date patient records and ensure data accuracy.
- Track and verify protocol amendments, EC/IRB approvals, and regulatory submissions.
- Report adverse events promptly and accurately.
Required profile
- Bachelor’s degree in a health‑related or biological field.
- Fluent in Hebrew with working proficiency in English.
- Israeli citizenship or full legal working rights in Israel.
- Previous experience as a clinical study coordinator is an advantage.
Required skills
- Good Clinical Practice (GCP) knowledge.
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Published 21 hours ago
Expires 1 month from now
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Soroka Medical Center
Beer-Sheva
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