Regulatory and Start Up Specialist - Fluent in Hungarian
Precision for Medicine · Slovakia
Regulatory Affairs
Remote
physician
Nurse
Pharmacist
Demand80
Career growth75
Healthcare fit85
Remote potential70
5-year outlook
Regulatory/start-up specialists in CROs have stable demand; with experience, progression to Regulatory Lead or Manager roles can improve compensation, though exact figures vary by country and CRO.
Clinical license
Not required
Applicant reach
narrow
Seniority
mid
Employment type
full-time
Date found
2026-10-03
Intelligence details
Flexible work details
- Side income
- Classified as side-income friendly
- Engagement type
- Contract
- Hours
- Variable hours
- Profession fit
- physician, Nurse, Pharmacist
- Rate period
- Annual
Why this was classified this way
- Contract
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
A strong non-clinical option for Hungarian-speaking clinicians with CRO/regulatory exposure; not suitable for those without prior start-up or regulatory experience.
Who should apply
Nurses, pharmacists, or life sciences graduates with CRO/pharma regulatory or start-up experience and fluent Hungarian.
CV angle
Emphasize clinical trial regulatory submissions, ethics committee/competent authority interactions, site activation, essential document collection, ICH-GCP, and Hungarian language skills; frame clinical experience as transferable to regulatory coordination.
Skills to highlight
- Regulatory submissions
- Clinical Trial Applications
- Ethics Committee submissions
- Site activation
- ICH-GCP
- TMF management
- Stakeholder communication
- Hungarian fluency
Role summary
Manage regulatory and start-up activities for clinical trials in Hungary, including CTA submissions, ethics committee approvals, site activation, and essential document collection.
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