Partner with Indero’s Clinical Monitoring Team
Indero is a dual focus CRO for dermatology and rheumatology clinical trials that ensures study compliance through risk-based clinical monitoring services. Tell us about your clinical trial needs.
Risk-based clinical monitoring services that ensure dermatology and rheumatology clinical trials run according to protocol and regulatory requirements.
To ensure participant safety, data integrity, and trial success, our clinical monitoring team undergoes the same training and testing as investigators for efficacy assessments (EASI, IGA, PASI, SALT, etc.). This rigorous training enables clinical research associates (CRAs) to quickly identify potential risks and escalate them to skilled clinical trial managers, ensuring a deep understanding of the efficacy evaluations they monitor. Also, our clinical monitoring team follows an adaptive (risk-based) approach, which emphasizes on-site monitoring efforts informed by the review of identified critical data and processes, issues, and trends. As a niche CRO specialized in dermatology and rheumatology, our CRAs and central monitors are highly trained and experienced in these therapeutic areas.
Risk Assessment
We systematically evaluate critical data and process risks associated with the protocol.
Site Management
We develop a unified, cross-functional plan to monitor identified trial risks.
Continuous Analysis
We integrate emerging risks, iteratively adapt the monitoring plan, and improve oversight in real time.
On-Site Monitoring
We investigate and address emerging process-related risks and concerns that can only be performed on-site.
Remote Monitoring
We remotely investigate and address emerging process or data-related risks and concerns.
Central Monitoring
We aggregate and analyze data to identify risks and trends and provide direction to monitoring activities.
Experience
The average clinical monitoring team member has over 15 years of industry experience working in the clinical research industry.
Established Relationships
Our team has established working relationships with thousands of dermatology and rheumatology sites, making on-site monitoring visits seamless. Our familiarity with site processes fosters site engagement and recruitment.
Indero is a dual focus CRO for dermatology and rheumatology clinical trials that ensures study compliance through risk-based clinical monitoring services. Tell us about your clinical trial needs.
Learn more about how our clinical team works with our adaptive clinical monitoring approach.
Site Monitoring Visits
Site Management
Centralized Monitoring
Scientific discipline. Operational efficiency. Clinical development expertise. Our clinical monitoring services provide the rigorous foundation, quality data, and expertise dermatology and rheumatology studies need to ensure effective execution and on-time delivery.
“My work experience with Indero has been very positive. Their monitoring support has been crucial in achieving our research goals. So far, this partnership is a true success story. Their professionalism and expertise are commendable.”
Copernicus Medical Center, Gdansk
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Our long-standing relationships with key opinion leaders and highly performing sites result in optimized start-up processes that deliver strong results in the least amount of time. As part of our site evaluation, our team utilizes past performance metrics, recruitment projections based on the competitive landscape, and detailed feasibility surveys to determine a site’s capabilities and interest in a study.
Our dedicated patient recruitment and advertising team integrates with the study team to tailor recruitment strategies, customize central ad campaigns, develop advertising creative, and continuously track and adapt recruitment goals. Our patient-centric approach is enhanced by Clinago, our technology enabled recruitment service.
We orchestrate all study activities and deliverables, including the site selection process, budget and contract negotiations, patient engagement, and recruitment enrollment projections, all while respecting your study timelines.
We orchestrate all study activities and deliverables, including the site selection process, budget and contract negotiations, patient engagement, and recruitment enrollment projections, all while respecting your study timelines.
