Study Start-up Specialist
BeiGene · Spain
Clinical Research
Remote
physician
Pharmacist
Demand78
Career growth75
Healthcare fit82
Remote potential55
Salary band
EUR 46k – 58k
5-year outlook
Mid-level clinical research role with a listed Spain salary range of 46,100–57,600 EUR. Progression toward Clinical Trial Manager, Start-up Lead, or regional clinical operations roles can increase compensation, though exact figures depend on country, CRO/pharma market, and experience.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-09-28
Intelligence details
Flexible work details
- Side income
- Classified as side-income friendly
- Engagement type
- Contract
- Hours
- Variable hours
- Profession fit
- physician, 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
Worth applying for clinicians with CRO/pharma start-up experience, especially multilingual Spanish/Portuguese speakers. Less suitable for clinicians without clinical research operations exposure because the role requires prior start-up experience.
Who should apply
Physicians, nurses, pharmacists, or healthcare graduates with 2+ years in clinical trial start-up, CRO, or pharma; multilingual English/Spanish/Portuguese speakers; professionals interested in oncology research and site-facing clinical operations.
CV angle
Frame clinical experience as transferable to trial start-up: site coordination, regulatory documentation, ICH-GCP, informed consent, ethics/HA submissions, quality review, and multilingual site communication. Quantify study/site volumes, timelines, and compliance outcomes where possible.
Skills to highlight
- Clinical trial start-up
- Regulatory submissions to EC/HA
- ICH-GCP compliance
- Informed Consent Form management
- Site activation and essential document reconciliation
- Budget and contract negotiation support
- IVDR compliance
- Inspection readiness
- Spanish/Portuguese/English communication
Role summary
The Study Start-up Specialist manages and coordinates clinical trial start-up activities across multiple sites, including regulatory submissions, informed consent adaptation, site document collection, budget/contract support, quality review, and inspection readiness. The role works closely with investigators, physicians, and research teams and requires strong knowledge of ICH/GCP and country-specific regulations.
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