Regulatory and Start Up Specialist - Spain
IQVIA · 2 Locations · Global
Clinical Research
–
Not yet analysed
Demand70
Career growth66
Healthcare fit72
Remote potential45
5-year outlook
CRO regulatory and study start-up roles typically pay in a stable mid-range band, with meaningful uplift on progression to Senior Start-Up Lead, Regulatory Affairs Manager, or Clinical Trial Manager. Compensation growth is steady but rarely explosive; sponsor-side or specialist regulatory roles tend to pay more than CRO delivery roles.
Clinical license
Not required
Applicant reach
moderate
Seniority
unclear
Employment type
–
Date found
2026-09-28
Intelligence details
Why this is worth applying to
Worth considering if you want a structured entry into clinical research operations and already have some exposure to trials, GCP, or site documentation. The posting is too thin to judge level or pay, so verify scope, seniority, and location terms before investing time.
Who should apply
Physicians, nurses, pharmacists, and IMGs with prior clinical trial, research coordinator, or site-level documentation experience who want a non-patient-facing CRO career; healthcare graduates with GCP training and strong Spanish/English writing skills.
CV angle
Reframe real clinical experience around trial-adjacent outputs: ethics/IRB or institutional review exposure, informed consent and protocol documentation, patient recruitment and screening logs, source data and essential document handling, and coordination with multiple stakeholders. Quantify site or study volumes, timelines met, and audit/inspection readiness. Lead with GCP training, regulatory submission familiarity, and bilingual communication — do not claim regulatory filing authority you have not held.
Skills to highlight
- ICH-GCP and clinical trial documentation
- Regulatory and ethics committee submission preparation
- Site activation and study start-up coordination
- Essential documents and eTMF management
- Stakeholder coordination across sites, sponsors, and vendors
- Protocol and informed consent review
- Attention to detail and deadline management
- Spanish and English written communication
Role summary
A CRO-based study start-up position at IQVIA Spain covering regulatory and ethics submissions, site activation, and essential document collection to get clinical trials open and enrolling. It is a documentation- and coordination-heavy clinical research operations role with no direct patient care.
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