Regulatory and Start Up Specialist - Israel
IQVIA · Tel Aviv, Israel · Global
Regulatory Affairs
–
Not yet analysed
Demand68
Career growth62
Healthcare fit70
Remote potential40
5-year outlook
CRO regulatory/start-up roles typically offer stable, mid-range professional salaries with incremental growth as you move from specialist to lead/manager or into broader regulatory affairs. Exact figures vary by country, experience and CRO, and cannot be confirmed from this posting.
Clinical license
Not required
Applicant reach
moderate
Seniority
unclear
Employment type
–
Date found
2026-10-19
Intelligence details
Why this is worth applying to
Worth considering if you are Israel-based and want a structured entry into CRO regulatory and clinical trial start-up work — a well-trodden path out of clinical practice. Because no description was supplied, verify the actual experience level, language requirements and hybrid expectations before investing time.
Who should apply
Israel-based clinicians (physicians, nurses, pharmacists, allied health) and IMGs/healthcare graduates with GCP exposure or research coordinator experience who want to move into CRO regulatory affairs or site start-up. Particularly suited to detail-oriented people comfortable with documentation, timelines and regulator/ethics committee correspondence.
CV angle
Reframe real clinical experience around documentation accuracy, protocol adherence, ethics/IRB or hospital committee exposure, audit and inspection readiness, and multi-stakeholder coordination with sponsors, sites and regulators. Highlight any trial participation, GCP training, patient recruitment or data collection work, and state language proficiency (Hebrew/English) explicitly — do not claim regulatory submission experience you do not have.
Skills to highlight
- Regulatory and ethics committee documentation
- ICH-GCP and protocol compliance
- Clinical trial site coordination
- Essential document management and audit readiness
- Stakeholder communication with sponsors and sites
- Attention to detail and timeline management
- Hebrew and English communication
- Feasibility and site selection support
Role summary
A CRO-based role at IQVIA supporting clinical trial regulatory submissions and site start-up in Israel — preparing and tracking ethics/regulatory packages, essential documents and site activation activities so studies can begin on time. Full duties are not included in the posting.
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