Regulatory affairs
| Highest | $9,000 / mo · United States |
|---|---|
| Experience | 5+ yrs |
| Degree | Required |
| First paycheck | 5 years of study (BSc) or 4 years BSc + 2 years MSc |
Pay in the destination countries
Monthly, in US dollars. Each country is an Imora admission package — open one for that route's fees, language requirement and deadline.
| Country | Monthly |
|---|---|
| United StatesTOEFL 80–100 · $10–70k | $9,000max |
| Hong KongIELTS 6.0–6.5 · HK–200k | $8,550 |
| SingaporeIELTS 6.5 · SGD 18–35k | $8,550 |
| United KingdomIELTS 6.0–7.0 · £11–38k | $8,550 |
| SwitzerlandIELTS 6.5 · CHF 0.9–8k | $8,300 |
| CanadaIELTS 6.0–6.5 · CAD 20–40k | $8,300 |
What does the day look like?
Your day is 100% office-based or remote computational work. 50% of your working hours are spent drafting, reviewing, formatting, and technically validating regulatory dossiers such as Marketing Authorisation Applications (MAAs), New Drug Applications (NDAs), and eCTD variation packages across Modules 1 to 5. You work in specialised software like Veeva Vault RIM Suite, OpenText Documentum, EXTEDO eCTDmanager, or LORENZ docuBridge, validate submissions with EURS is-valid or Lorenz eValidator, and audit packaging texts with TVT.
Cross-functional strategy meetings with R&D, clinical, and legal teams take 25% of your time, health authority correspondence via gateways like the FDA ESG or EMA portal takes 15%, and system archival takes 10%. Standard hours are 37.5 to 40 hours per week, Monday through Friday. There are no night shifts, no on-call rotas, and 0% wet laboratory work. Overtime occurs occasionally in the evenings ahead of strict agency submission deadlines.
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