Win more studies.
Design trials that recruit.
Deliver with confidence.

Connected clinical intelligence that helps CRO teams win proposals, pressure-test feasibility, and de-risk recruitment before delivery.

Prefer to talk it through? Speak to a clinical planning expert

Evidence, not assumptions. From proposal through delivery.

From patient intelligence and protocol planning through feasibility, site selection, competitive benchmarking and recruitment support, Citeline helps CROs make faster, more defensible decisions across the clinical development workflow.
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Data-backed insights

Objective clinical and competitive intelligence behind every recommendation

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One connected workflow

From patient reality through feasibility, sites, and recruitment

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Expert-curated, AI-enabled

Human-curated intelligence with AI-enabled analytics you can defend

How Citeline Helps

Win the work. Plan it well. Deliver with confidence.

Win more competitive RFPs

Build stronger proposals supported by objective evidence, competitive landscapes, recruitment benchmarks, and therapeutic-area insight.

  • Differentiated, data-backed RFP responses
  • Competitive landscapes for bid defenses
  • Therapeutic-area and recruitment benchmarks

Benchmark against what success looks like

Compare trial designs, endpoints, timelines, enrollment patterns, and geographic activity to inform more defensible recommendations.

  • Trial design and endpoint benchmarks
  • Realistic timeline and enrollment patterns
  • Country and site activity comparisons

Design studies that recruit

Leverage AI to bring patient reality into planning earlier, so protocol design, feasibility, and recruitment strategies are aligned from the start.

  • Understand how eligibility affects patient availability
  • Find where protocol-matched patients and HCPs may be
  • Reduce downstream recruitment delays

One connected workflow, three ways it pays off

Winning strategies from the start, and faster, defensible options for at-risk studies.

Win

Stronger, evidence-backed proposals and bid defenses

Plan

Feasibility and recruitment assumptions grounded in real data

Deliver

Faster, defensible options when studies are at risk

Move from fragmented planning to connected clinical intelligence

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Patient reality

Understand eligible populations, treatment pathways, and where protocol-matched patients may exist.

Protocol design

Pressure-test whether eligibility criteria, endpoints, and assumptions support a recruitable study.

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Feasibility and planning

Benchmark trial designs, timelines, countries, and enrollment expectations against real-world trial intelligence.

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Site and investigator selection

Identify sites and investigators with relevant experience, access, and performance potential.

Recruitment execution

Support targeted recruitment strategies and patient identification earlier in the planning workflow.

Competitive monitoring

Track trial activity, sponsor behavior, endpoints, timelines, and market movement.

Recovery & Efficiency

When timelines slip, find the next best move

When recruitment is behind plan or site performance is weaker than expected, reassess the landscape, identify alternative countries and investigators, and refine recruitment strategies using objective intelligence sponsors can trust.
Validate country, site, timeline, and enrollment assumptions using clinical trial intelligence and performance benchmarks, connected to the broader workflow.
Support recruitment planning and patient identification with data-led insight into protocol-matched populations and referral opportunities, both upstream and downstream.
Access expert-curated intelligence, analytics, and specialist support without building bespoke internal teams for every indication or RFP, protecting billable capacity.
SmartSolutions dashboard showing recommended investigators based on filtered criteria.
PRICING

Find the right Citeline package for your team

Speak to a Citeline expert to discuss your use case, access needs, and the right setup for your organization.

Content

Explore further resources

Frequently Asked Questions

By supporting proposals and bid defenses with objective evidence, competitive landscapes, recruitment benchmarks, and therapeutic-area insight, so responses are differentiated and sponsor-ready.
Yes. Much recruitment risk is created at protocol design and feasibility. Citeline brings patient reality into planning earlier so eligibility, feasibility, and recruitment strategies align from the start.
When recruitment is behind plan or site performance is weak, teams can reassess the landscape, identify alternative countries and investigators, and refine recruitment strategies with evidence sponsors can trust.
Business development, proposal, feasibility, clinical operations, recruitment, therapeutic-area experts, and executive leadership, each with a different best-fit angle across the workflow.
Citeline connects intelligence across patient reality, protocol design, feasibility, site selection, recruitment, and competitive monitoring, rather than offering disconnected point tools.
AI-enabled analytics are grounded in expert-curated clinical intelligence, proprietary performance data, and real-world data, so recommendations can be defended in front of sponsors.

Speak to the Citeline CRO team

Compete, plan, and deliver with confidence. Tell us what you're working on, and our team will be in touch shortly.

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