Market notes
European employers often look for EU/EEA or UK right to work. Where the role can be performed remotely or from an offshore centre, India-based specialists are a practical option.
EU and UK data-protection rules apply to candidate data. We handle consent in layers and put data-transfer terms in place with EU and UK clients.
Some roles carry location conditions by law, for example the EU qualified person for pharmacovigilance must be based in the EU/EEA.
Regulators and frameworks
- EMA
- National competent authorities
- MHRA (UK)
Typical mobility
- Existing right to work
- Employer-sponsored relocation
- Remote or offshore delivery
Specialisms we cover here
Clinical Research
CRAs, trial managers, start-up.
Pharmacovigilance
Safety scientists, ICSR and aggregate-report specialists, signal detection.
Regulatory Affairs
CMC, labelling, eCTD publishing, submissions.
Quality Assurance
GMP, GCP and GVP audit, QMS, validation.
Medical Writing
Protocols, CSRs, CTD modules, publications.
These notes are general orientation, not legal, tax or immigration advice.