Clinical Monitoring

Clients seek Linical out due to their quality of clinical monitoring. Clinical monitoring is essential to ensure patient protection, regulatory compliance, data quality, and integrity of your clinical trial’s results.

Linical provides global monitoring and site management solutions to our clients via our international team of experienced professionals. 

Lorem ipsum dolor sit amet, consectetur adipiscing Linical CRAs have a minimum of five years' industry experience prior to joining our organization and are knowledgeable in all aspects of study conduct. Our CRAs are highly skilled, therapeutically aligned, centrally trained, and committed to excellence in every study. We are agile and can recommend remote, decentralized, hybrid or onsite depending on your need.

With Linical, you get CRAs that are dedicated to your project, have direct access to executive management, and use efficient processes to streamline your clinical study conduct.


Clinical Trial Monitoring & Site Management Services

Linical’s Clinical Research Associates (CRAs) are your dedicated eyes and ears throughout your study, ensuring the integrity of the study, adherence to protocol, quality of measurements, and safety of patients. Our monitoring team reviews and verifies essential documentation related to the study to confirm accuracy and completeness, thereby certifying that the data collected in the clinical trial is reliable and complies with all applicable regulations, ethics, and guidelines.

Linical provides global monitoring and site management solutions through an international team of experienced CRAs deployed in major clinical trial markets in North America, Europe and Asia. Our monitoring plans, prepared by the Clinical Trial Manager and approved by the Project Manager, cover all details related to:


Monitoring Visits
Including anticipated timing of the visits and source data verification requirements; project-specific monitoring report completion and approval turnaround times
Site Management
Including communication, investigational product receipt and resupply, randomization procedures and reporting serious adverse events and protocol deviations
Trial Master File (TMF) Management
Maintaining high-quality, inspection ready study documentation

Site Management at it’s Finest

Linical’s CRAs engage each site from initiation to close-out, performing: training, remote and on-site review of data, query management, support in logistical matters, day to day protocol questions, and preparation and collection of all required documents.

We have forged strong bonds with top performing clinical research sites and long-term relationships with site staff; this allows us to easily tailor communications and receive timely updates from the Principal Investigator (PI) and study coordinators, developing a site-specific recruitment plan and offering guidance and support to address any barriers the site may be experiencing on an ongoing basis. In addition, Linical uses industry-leading technology to facilitate remote monitoring between visits, ensuring that issues are addressed promptly, sites remain actively engaged, and that our time on site is used as efficiently as possible.

Right Size
Right Reach
Right Team

Flexible Clinical Monitoring Solutions

Linical’s monitoring services include:
On-site Visits
Including source-data verification and monitoring reports
Remote Visits
Including remote review of source documents using established methods for secure file transfer
Traditional 100% SDV or Risk-based Monitoring Flexibility
Flexible clinical trial monitoring approaches to fit your study goals

Why Linical?

The clinical development journey can be daunting and often leads to failure. With so much riding on your compound, you deserve the best chance at achieving your goals and positively impacting patients across the globe.

As a global, award-winning CRO, we can provide the strategy and support you need to position your clinical trial for success. We have an impressive track record of exceeding our enrollment goals and maintaining nearly a 90% client retention rate.

With our collaborative approach and commitment to quality, Linical expertly guides you through each step of the process, from early-phase research to large-scale global studies. With Linical, you can overcome obstacles, expedite timelines, save valuable money, and achieve your goals without compromising quality.

Cultivating The Top Clinical Research Professionals

Linical has developed a specialized CRA Training Academy as well as a Study Coordinator to CRA Bridging program, where we select talented professionals and cultivate their skills through an extensive training program on all facets of clinical research and trial oversight. This unique program allows us to introduce more individuals to clinical research careers, and increases our pool of skilled CRAs to support clients' programs.

Successful clinical trials start with Linical.

Don’t let the complex clinical development journey hold you back. With Linical, you can overcome obstacles, save valuable time and money, and reach your goals. 

01 Request a proposal

We start by listening to your needs and understanding your goals to ensure we’re the right CRO for you.

02 Get a plan for success

We propose solutions that proactively tackle obstacles, optimize your trial design, and position you for success every step of the way.

03 Execute with confidence

We’ll guide you through each phase of the process, offering personalized support and a full range of services to help you achieve a successful trial. We are not a “one size fits all” CRO.

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