What we do

Clinical Research Operations (CRO)

From trials to trust. From science to solutions.

Add 2–3 outcome bullets here (speed, quality, access, evidence).
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Replace with team-in-action photo or abstract clinical imagery.

Why it matters

Short narrative: what problem CRO solves, who it’s for, and why VIR’s approach is different. Keep it to 2 paragraphs max.

Capabilities

Infographic + structured list
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Use a grid of icons for: Study Design, Operations, Data, QA, Safety, Writing, RWE, Tech.

Areas we support

  • Study Design & Strategy: protocol, feasibility, regulatory strategy
  • Clinical Operations: interventional + non‑interventional management
  • Data Management & Analytics: validation, biostats, reporting
  • Safety & Medical Oversight: monitoring, AE reporting
  • Regulatory & QA: ethics submissions, GCP compliance
  • Medical Writing: CSRs, publications, value storytelling
  • Market & Real‑World Insight: observational, post‑marketing
  • Technology & Innovation: EDC, dashboards, remote monitoring

How we work

1) Discover

Goals, constraints, stakeholders

2) Design

Protocol + operational plan

3) Execute

Run study with oversight

4) Communicate

Outputs + evidence story

Proof

Use anonymized case cards if needed

Case study (anonymized)

Challenge → Approach → Outcome (3 bullets). Replace with real.

Case study (anonymized)

Challenge → Approach → Outcome (3 bullets). Replace with real.

Contact

Let’s plan your study.

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