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Maxis AI — THE FIRST AI WORKFORCE IN CLINICAL TRIALS
For Mid-Sized Pharma

Agentic AI for Mid-Sized Pharma

Run governed, AI-driven trials with the throughput of a top-20 sponsor.

Mid-sized pharma teams operate with lean internal capacity, heavy CRO dependence, and fixed milestone pressure across multiple programs.

Maxis AI provides a supervised execution layer that strengthens internal capability — improving biometrics throughput, predictability, and oversight without expanding contractor spend.

Human-in-the-loop validation · Audit traceability

STUDY THROUGHPUT · LIVE
Database Lock↓ 42% cycle
Query Resolution↓ 60% time
Submission Readiness↑ 2.1× speed
Risk Coverage100% sites
12
Trials
4.2×
Velocity
$1.8M
Saved
Agentic AI Offerings

Our platform strengthens execution across critical workflows.

Study Startup Coordination

  • Faster site activation readiness
  • Improved startup tracking visibility

Clinical Data Management

  • Automated data cleaning and validation
  • Reduced manual reconciliation effort

Statistical Programming Support

  • Improved biometrics efficiency
  • Automated dataset preparation

Portfolio Oversight

  • Continuous monitoring across trials
  • Earlier detection of execution risks
Operational Pressure

Where Mid-Sized Pharma Execution Slows

Execution gaps commonly occur due to:

Heavy reliance on CRO partners

Limited internal biometrics capacity

Delayed database readiness timelines

Fragmented operational visibility

Small teams managing large portfolios

Outcomes

What Improves with Agentic AI

With Agentic AI for mid-sized pharma, execution becomes structured and predictable.

Faster database readiness and submission timelines

Improved biometrics efficiency without contractor expansion

Earlier detection of risks across programs

Stronger execution visibility across CRO and in-house workflows

Improved milestone predictability

Recommended Approach

Deploy the AI Workforce across data management and statistical programming workflows first — the highest capacity constraints. Organizations that do this recover 40–50% of database lock time without expanding teams.

Case Study

12 FTEs. 15 Trials. No Contractors. DB Lock Accelerated 40–50%.

80% manual query effort. SAP cycles stretched to 4–8 weeks. See how a mid-sized pharma scaled biometrics execution without adding headcount.

15 Trials

Managed by 12 FTEs

60–70%

Queries auto resolved

40–50%

Faster DB lock

0

Contractors hired

FAQ

All You Need to Know

It embeds supervised execution across biometrics and clinical workflows, improving readiness visibility and throughput consistency.

It allows execution capacity to scale independently of biometrics staffing while maintaining governance controls.

Through unified portfolio oversight, traceable workflows, and structured supervision thresholds.

Biometrics efficiency, governance visibility, and database readiness timelines.

By coordinating structured workflows under governance controls, improving execution predictability across regions and partners.

Looking for Agentic AI for clinical trials?

Explore the Agentic AI Platform.

See how AI agents are transforming study startup, data management, oversight, and regulatory submissions.