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.
We cover all the different hiring needs you might have
Technology areas we staff for pharmaceutical and life sciences
- GxP-compliant application development and computer system validation (CSV)
- Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC)
- Laboratory Information Management Systems (LIMS)
- Regulatory submission technology (eCTD, Veeva Vault, IDMP)
- ERP for pharmaceutical manufacturing (SAP, Oracle)
- Pharmacovigilance and drug safety systems
- Life sciences data engineering and clinical analytics
- Cloud infrastructure for regulated environments (AWS GxP, Azure for Life Sciences)
Why companies choose Fast Dolphin for pharmaceutical IT staffing
Search, screening, and shortlisting handled
You only evaluate candidates who have been assessed for technical fit, pharmaceutical system experience, and regulatory awareness.
We manage hiring and compensation
Fast Dolphin handles employment, payroll, and compliance so your IT professionals can contribute to your programs from day one.
Full time zone overlap
Our professionals work from Latin America in your business hours, enabling real-time collaboration on validation projects, regulatory timelines, and clinical data work.
GxP and life sciences system experience
We source professionals with hands-on experience in validated environments, GxP-aligned development, clinical systems, and regulated data management.
Expert guidance during selection
We advise on role scope, system-specific availability, and seniority benchmarks for pharmaceutical IT profiles before you finalize a brief.
On-site, remote, or hybrid
Placements are available across all work models, including on-site for roles requiring physical presence at your facility or manufacturing site.
Flexible engagement duration
Pharmaceutical programs shift with clinical milestones and regulatory cycles, and engagements can be extended or concluded with proper notice.
Frequently Asked Questions​
What pharmaceutical IT roles can Fast Dolphin staff?
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.
How does Fast Dolphin handle GxP and regulatory compliance awareness in its placement process?
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.
Can Fast Dolphin staff for both commercial pharmaceutical companies and CROs?
Yes. We place for pharmaceutical manufacturers, biotechnology companies, contract research organizations (CROs), and contract manufacturing organizations (CMOs) across both commercial and clinical-stage operations.
Do your pharmaceutical IT professionals work in US business hours?
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.