Regulatory and Start Up Specialist
Precision Medicine Group · United Kingdom · GB
Regulatory Affairs
Remote
physician
Nurse
Pharmacist
Demand78
Career growth74
Healthcare fit84
Remote potential55
5-year outlook
Likely a stable mid-level CRO/regulatory career with progression toward Start-Up Lead or Regulatory Lead; compensation growth depends on UK market conditions and prior submissions experience, without a guaranteed figure.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-10-26
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 applying if you have clinical trial, regulatory, or site coordination exposure and want a CRO regulatory/start-up pathway; less suitable for clinicians with no research or submissions experience.
Who should apply
Nurses, pharmacists, doctors, or healthcare graduates with clinical trial, ethics/IRB, site activation, regulatory, or research coordination experience, especially those familiar with UK submissions.
CV angle
Frame real clinical/research work around regulatory dossier preparation, ethics/CA interactions, site activation timelines, essential document/TMF management, GCP, and stakeholder coordination; quantify timelines and submissions only where true.
Skills to highlight
- Regulatory submissions
- Clinical Trial Applications
- Ethics Committee/IRB coordination
- ICH-GCP
- Site activation and start-up
- Essential document collection and TMF management
- Stakeholder communication
- Contract and budget negotiation support
Role summary
Coordinates country/site regulatory submissions and start-up activities for clinical trials, including CTA/ethics dossiers, site activation, essential documents, and contract/budget support.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.