United States
Remote and offshore specialists, plus candidates with existing work authorisation.
Market notes
US employers hire the full range of functions. For candidates outside the US, work authorisation is the main constraint, so we state it up front on each profile.
Many US sponsors and CROs use offshore teams for safety, medical writing and regulatory operations. That is where our India sourcing is most useful.
Please note. We do not give immigration advice. Work authorisation is the employer’s responsibility to verify.
Regulators and frameworks
- FDA
- DEA (controlled substances)
Typical mobility
- Existing US work authorisation
- 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.