Regulatory and Start Up Specialist
Precision for Medicine · United Kingdom · GB
Regulatory Affairs
Remote
physician
Nurse
Pharmacist
Demand78
Career growth72
Healthcare fit84
Remote potential60
5-year outlook
Likely a stable CRO regulatory/start-up pathway with pay progression as UK regulatory and site activation expertise deepens; compensation varies by employer, seniority, and hybrid/remote arrangement.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-10-25
Intelligence details
Flexible work details
- Side income
- Classified as side-income friendly
- Engagement type
- Contract
- Hours
- Variable hours
- Eligible countries
- United Kingdom
- License jurisdiction
- GB
- 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
Worth considering for clinicians with clinical trial site, GCP, or research coordination exposure who want a CRO regulatory/start-up pathway; less competitive if you have no regulatory submission or site activation experience.
Who should apply
UK-based nurses, pharmacists, allied health professionals, doctors, or healthcare graduates with clinical trial, research site, GCP, or regulatory documentation experience, especially those interested in CRO start-up and site activation.
CV angle
Translate clinical experience into regulatory/start-up language: ethics/IRB submissions, informed consent, essential documents, site activation, GCP compliance, audit readiness, stakeholder coordination, and timeline tracking. Emphasize any real exposure to CTA/regulatory dossiers, site contracts, budgets, or TMF without overstating.
Skills to highlight
- Regulatory submissions
- Clinical Trial Application preparation
- Ethics Committee and Competent Authority interactions
- ICH-GCP compliance
- Site activation and start-up
- Essential document management
- Informed consent customization
- TMF/audit readiness
Role summary
Country-level clinical trial regulatory and start-up role supporting CTA/ethics submissions, site activation, essential documents, and site contract/budget coordination for a CRO.
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