Nearshore Pharmaceutical IT and Engineering Staffing
Clinical timelines and compliance don't leave room for slow hiring
Pharmaceutical and life sciences companies operate under some of the most demanding regulatory frameworks in any industry. From GxP-compliant system validation and clinical data management to SAP implementations and regulatory submission technology, the IT professionals needed to support these environments are both highly specialized and difficult to find in North America. Fast Dolphin places experienced IT and engineering professionals from Latin America with US and Canadian pharmaceutical and life sciences organizations, across any staffing model you need.
You only evaluate candidates who have been assessed for technical fit, pharmaceutical system experience, and regulatory awareness.
Fast Dolphin handles employment, payroll, and compliance so your IT professionals can contribute to your programs from day one.
Our professionals work from Latin America in your business hours, enabling real-time collaboration on validation projects, regulatory timelines, and clinical data work.
We source professionals with hands-on experience in validated environments, GxP-aligned development, clinical systems, and regulated data management.
We advise on role scope, system-specific availability, and seniority benchmarks for pharmaceutical IT profiles before you finalize a brief.
Placements are available across all work models, including on-site for roles requiring physical presence at your facility or manufacturing site.
Pharmaceutical programs shift with clinical milestones and regulatory cycles, and engagements can be extended or concluded with proper notice.
We place GxP application developers and CSV specialists, CTMS and EDC engineers, LIMS administrators, regulatory submission technology professionals (Veeva Vault, eCTD), SAP and Oracle consultants with pharmaceutical industry experience, pharmacovigilance system specialists, life sciences data engineers, and cloud engineers with experience in regulated environments.
Regulatory context is incorporated into our candidate briefing and screening criteria. For pharmaceutical roles, we evaluate prior GxP experience, CSV knowledge, and familiarity with relevant regulatory frameworks such as FDA 21 CFR Part 11, EU Annex 11, and ICH guidelines.
Yes. We place for pharmaceutical manufacturers, biotechnology companies, contract research organizations (CROs), and contract manufacturing organizations (CMOs) across both commercial and clinical-stage operations.
Yes. Our professionals are based in Latin America and work in alignment with US and Canadian business hours, supporting validation cycles, regulatory submission timelines, and clinical data management in real time.