Market notes
India is a deep source of pharmacovigilance, clinical operations, medical writing and regulatory operations talent, and many global companies run delivery centres here.
Notice periods are often long. We confirm notice and buy-out flexibility on the first call so timelines are realistic.
We hire for in-country roles and also introduce India-based specialists to employers abroad, either for remote and offshore work or for relocation.
Regulators and frameworks
- CDSCO
- PvPI
- State licensing authorities
Typical mobility
- In-country hire
- Remote or offshore role for a non-Indian employer
- Outbound relocation (employer-led)
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.