IT Staffing › Healthcare

Healthcare Talent, Placed by People Who Know It

Domain knowledge isn't a bonus here, it's the baseline. We staff healthcare roles across clinical, regulatory, pharmacovigilance, and life-sciences technology.

in
Microsoft
DevOps Engineer
Part-time Senior level
$130/hr
Seattle, WA, CA
in
Google
Cloud Engineer
Full-time Mid level
$145/hr
Mountain View, CA
in
Amazon
Software Engineer
Full-time Senior level
$155/hr
New York, NY
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2 weeks later
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Priyanka Sharma

DevOps Engineer

Kubernetes, Docker, Azure, CI/CD Pipelines

500+ connections

Open to work ✎

Trusted by teams at:

Clients logos

Services

Healthcare Data & Platforms

Specialists in the platforms, pipelines, and data systems that keep healthcare operations running.

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Data & AI for healthcare

Professionals who build and manage AI models and data pipelines purpose-built for clinical and healthcare environments.

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Veeva - Safety, Vault RIM,
Clinical (CTMS / eTMF)

Specialists across the full Veeva suite from pharmacovigilance workflows to regulatory submissions and clinical trial management.

Healthcare professionals using digital technology
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Medical coding - NDC / ICD

Certified coders fluent in NDC and ICD systems, keeping your clinical billing, compliance, and documentation audit-ready.

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PL/SQL migration & data quality

PL/SQL experts who handle structured data migration and quality assurance across your clinical and operational systems.

Healthcare Credentials

The groups behind our team

Here's how the two approaches compare — and why it matters for the engineers you end up with.

Class A/B/C + IVD

Class A/B/C + IVD

Group-owned medical-device manufacturing licenses, certified to ISO 13485:2016.

MDR/IVDR/EUrep

MDR/IVDR/EUrep

EUmAccess - EU Authorised Representative for MedTech, IVD & Diagnostics.

25+ in healthcare

25+ in healthcare

Specialist contractors placed and managed with a US healthcare MNC.

Process

Our Process Framework

How we deliver every engagement runs as a continuous loop.

Delivery

Our niche

The Roles That Separate Domain Experts From Everyone Else

Most staffing partners can't tell a medical writer from a CRA. We can because we've been doing this work ourselves.

Medical Writers 

The title "medical writer" undersells the job. The writing is the last 20% the real work is judgement about evidence. A good medical writer reads everything: trial data, published literature, guidelines, competing claims and decides what it will actually support.

They know the difference between a finding that survives a reviewer and one that gets torn apart, and they say so before it reaches the client. Which is why hiring for it is deceptively hard a writing sample tells you almost nothing; plenty of people write cleanly and reason badly. What you need to test is clinical literacy, research rigour, and the nerve to push back even when the deadline is tomorrow. That combination is rare, and we help you find it.

Pharma co-vigilance

Most staffing partners send you CVs filtered on keywords "MDR," "technical file," "4 years" and leave the actual judgement to your hiring manager. That's why your team burns hours screening people who shouldn't have reached the panel. We work differently because we do this work ourselves handling Class A, B, C and D manufacturing licences, MD-41 filings, EU Authorised Representative appointments, and EUDAMED.

So when we screen a regulatory affairs candidate, we're asking from inside the job: have they actually built a technical file, defended a risk classification, or seen a CDSCO query through to resolution? Those are questions a keyword filter can't ask and a non-domain recruiter can't score. That gives Terra a shorter shortlist, faster closure, and fewer early exits because we screen for scope upfront, not at week six. They know the difference between a finding that survives a reviewer and one that gets torn apart, and they say so before it reaches the client. Which is why hiring for it is deceptively hard a writing sample tells you almost nothing; plenty of people write cleanly and reason badly. What you need to test is clinical literacy, research rigour, and the nerve to push back even when the deadline is tomorrow. That combination is rare, and we help you find it.

Pharma co-vigilance

Medical regulatory

Think of medical device regulation less like getting a permit and more like being asked to prove your homework the manufacturer has to show the device is safe, and the regulator checks whether that proof and the system behind it are solid. In India, CDSCO sorts devices into four risk classes

A through D with licensing escalating from State authority for A and B, to Central authority in Delhi for C and D, and behind the licence you need a quality system, technical file, risk file, and a plant audit. Europe works the same way: Class I to III under MDR, a private Notified Body doing the audit, and a EUDAMED registration. In both places, the licence is just the start complaints get reported, files stay updated, and any design or supplier change puts you back in front of the regulator.

Medical regulatory

Ready to Hire?

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Tell us the role, the stack, and your timeline. We'll confirm fit within 24 hours and send your first shortlist shortly after.

Engineers network

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IT Staffing

Healthcare

Domain-deep hiring for clinical and regulatory roles medical writers, pharmacovigilance specialists, CRAs and many more, placed by people who understand the field.

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