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Empowering CROs with Efficient Recruitment and Operational Solutions

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Participant Recruitment and Pre-Screening

End-to-end recruitment services, including identifying potential participants and prescreening them based on study criteria.

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Customized Recruitment Campaigns

Tailored marketing and outreach campaigns designed to attract participants specific to each clinical trial’s needs.

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Regulatory Compliance Assistance

Ensuring all recruitment activities comply with local and international regulations

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Managing Existing Pool of Participants

Contacting existing participating and gathering missing information, ensuring comprehensive data collection and reducing the need for public recruitment

Patient Engagement and Retention

Implementing strategies to keep participants engaged throughout the trial, reducing dropout rates.

Multilingual Support

Providing recruitment and support services in multiple languages to reach diverse populations

Methodologies & Workflows

Data-Driven Recruitment

We leverage advanced analytics and machine learning algorithms to identify the most suitable participants for each trial. Our data-driven approach allows us to target and recruit participants efficiently, maximizing both speed and accuracy.

Custom Workflow Integration

We tailor our workflows to fit seamlessly within your existing processes. Whether it’s aligning with your data collection protocols or enhancing communication channels, our custom workflows are designed to complement and optimize your operations

Multi-Channel Outreach

Our recruitment strategies are executed through a multi-channel approach, including digital campaigns, community outreach, and direct engagement with existing patient databases. This ensures a broad reach and diversified participant pool.

Rigorous Pre-Screening:

Every potential participant undergoes a thorough pre-screening process to ensure they meet the study’s eligibility criteria. This step minimizes trial delays and ensures that only the most qualified candidates proceed to the next stage.

Continuous Monitoring & Reporting

Every potential participant undergoes a thorough pre-screening process to ensure they meet the study’s eligibility criteria. This step minimizes trial delays and ensures that only the most qualified candidates proceed to the next stage.

Our Database & Expertise

Age Diversity

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Participants aged 17-75 years

Diverse Representation

10+ ethnicities included

Participant Pool

5,000+ active participants

Comprehensive BMI Range

Participants with BMI 15-48

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Hepatic Impairment

Clinical Clear supports pharmacokinetic studies by providing CROs with a diverse database of participants with hepatic impairment. Our resources enable precise exploration of drug metabolism in liver-compromised individuals, facilitating the development of safe and effective treatments.

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Renal Impairment

We assist CROs in conducting pharmacokinetic studies by offering access to a carefully curated pool of participants with renal impairment. This support allows for accurate assessments of how varying kidney function impacts drug metabolism and clearance.

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Healthy Participants

To ensure comprehensive pharmacokinetic comparisons, Clinical Clear provides CROs with a reliable database of healthy participants. This resource is critical for establishing baseline metabolic profiles, enabling effective comparison with impaired populations.

Shows a healthcare professional pointing to a model of a kidney, with another person's hand also present, suggesting a medical explanation or consultation about kidney health.

Renal Impairment

We assist CROs in conducting pharmacokinetic studies by offering access to a carefully curated pool of participants with renal impairment. This support allows for accurate assessments of how varying kidney function impacts drug metabolism and clearance.

Group of people

Healthy Participants

To ensure comprehensive pharmacokinetic comparisons, Clinical Clear provides CROs with a reliable database of healthy participants. This resource is critical for establishing baseline metabolic profiles, enabling effective comparison with impaired populations.

Our Trials

30
%
Criteria completed
Open
New Drug
Fatty Liver
Rialto, California (92377)
3 months
More Details
100
%
Criteria completed
Closed
Contraceptive Methods
Females and Birth Control
Oral contraceptive
Healthy volunteer
Rialto, California (92377)
2 months
More Details
Show All Trials

Achievements and Growth With Our Partners

+40%

Fewer Screening Failures

+85%

Participant Retention Rate

+25%

Faster Timelines

2%

ROI

FAQ

What are the key differentiators of Clinical Clear compared to other recruitment services?
Can Clinical Clear provide support in multiple locations or states?
What is the typical recruitment timeline with Clinical Clear?
How does Clinical Clear ensure participant quality and eligibility?
How are Participants Protected?

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