Founded in 2015 in New Jersey, Kerlo Research is a collective of clinical research professionals dedicated to enhancing the industry. Through years of collaboration with top industry performers, we have expanded our service offerings to encompass study and site sourcing, study start-up assistance, patient management systems, educational courses, medical monitoring, and more. Our mission is to streamline the research process, fostering collaboration and achieving shared objectives across the clinical research landscape.

Services

Serving as a Clinical Research Organization, Kerlo Research provides a range of services that include, but are not limited to, the following areas:

• Clinical Trial Planning and Management
• Study Design and Feasibility
• Site Selection
• Regulatory Services
• Monitoring Services
• Data Management
• Patient Recruitment
• Medical Writing
• Drug Safety and Pharmacovigilance

Our team is composed of specialized subject matter experts and a cadre of highly skilled industry veterans. This wealth of expertise empowers us to tailor our offerings to each unique project, ensuring we meet and surpass our clients’ expectations.

Our reputation as dependable partners shines through in the intricate and fascinating pathways of development that our clients navigate in their research endeavors.

At Kerlo Research, we collaborate closely with your team to outline goals and devise cutting-edge strategies. We ensure there are clear Key Performance Indicators (KPIs) to measure progress. Our seasoned experts offer their skills to enhance your technological processes and operational efficiency.

Our team includes distinguished physicians, each with hands-on experience in conducting clinical studies across different therapeutic areas. They have served as Principal Investigators and Sub Investigators, enrolling patients and managing studies. Their expertise in clinical research proves invaluable in advisory roles, guiding our work on every project and offering creative solutions for complex challenges.

We cater our services to the specific requirements of each clinical project, whether as stand-alone options or under the full-service CRO model. This includes developing and commercializing new drugs and therapies in the US and globally. Additionally, we offer subcontracting support for major CROs, assisting with specific aspects of their projects they wish to outsource to Kerlo Research.

Kerlo Research’s adaptable strategies cater to businesses of all sizes

At Kerlo Research, we recognize the global nature of the industry, but we also understand that small to mid-sized companies may operate on a local scale due to limitations in expertise, financial capacity, or infrastructure.

A strategic partnership with Kerlo Research equips these firms with the advantages of a CRO that aligns with their vision and has the necessary expertise and reach for expansion into multiple international markets. Our balanced approach delivers unique cost-saving benefits.

Statistical data has demonstrated this method accelerates the growth of small firms, yielding a 22% increase in trial results. We are committed to providing the highest quality services while maintaining a flexible and responsive approach. Our goal is to be your partner in clinical research, not just another vendor.

Medical Monitoring Services: Our Comprehensive Approach

At Kerlo Research Clinical, we understand the challenges inherent in medical monitoring, including protocols lacking precise guidance, the absence of real-time data trackers to identify issues promptly, and the lack of a comprehensive Medical Monitoring Plan.

• Medical involvement in the development of study documents, protocols, training materials, and ensuring alignment and guidance.
• Evaluating subject eligibility.
• Providing guidance on medical matters and reviewing subject safety data.
• Assessing and reviewing protocol deviations and implementing mitigation plans, protocol amendments, and newsletters.
• Reviewing eCRF templates, eCRF instructions, and the Medical Monitor Plan.
• Contributing to safety review committees.
• Regular cross functional team meetings.
• Open communication with study sites.
• Track query responses assuring timely resolution.
• Understanding of services provided by the CRO/Vendors.
• Tailoring listings and patient profiles to align with data review objectives.
• Standardizing the data review process.

Following our commitment to addressing these challenges, we offer comprehensive services including Start-up, Ongoing Trial, and Close-out services to ensure seamless execution and successful outcomes for every clinical trial project.

Our cutting-edge medical monitoring services are powered by a state-of-the-art cloud-based software system developed by our esteemed IT team. This innovative solution is designed to streamline the data analysis process, significantly reducing both time and resources required. With our advanced technology, we can ensure quicker turnaround times, delivering results to sponsors promptly and efficiently. Welcome to a new era of medical monitoring excellence, where precision meets speed.