We are a global CRO delivering patient-centered clinical research solutions with a strong focus on quality, compliance and efficiency.
Clinara is led by a senior team of clinical research professionals with over a decade of experience delivering Phase I–IV clinical trials across diverse therapeutic areas including oncology, cardiovascular, CNS, endocrine, hematology, and infectious diseases. Combining deep scientific expertise with operational excellence, Clinara brings strong capabilities in trial planning, site activation, monitoring, and study close-out while maintaining the highest standards of compliance through ICH-GCP and global regulatory frameworks including FDA and Health Canada (TPD). The team specializes in risk-based monitoring, protocol adherence, adverse event management, and audit readiness, ensuring patient safety and data integrity throughout the study lifecycle. Acting as a true partner to sponsors, investigators, and research sites, Clinara drives seamless coordination, clear communication, and efficient execution, supported by strengths in training, budgeting, and clinical operations—delivering high-quality, compliant, and results-driven clinical trial outcomes.
Ahmad Shaheen is a Certified Clinical Research Professional (CCRP) with over 20 years of experience leading and supporting Phase I–IV clinical trials across sponsor, CRO, and site settings. His expertise spans clinical trial operations, regulatory compliance, patient recruitment, monitoring oversight, and quality execution, with deep knowledge of ICH-GCP, Health Canada Division 5, FDA/TPD regulations, and audit readiness. Ahmad has worked across a broad range of therapeutic areas including oncology, cardiovascular, CNS, endocrine, dermatology, infectious disease, and gastrointestinal research, bringing strong operational leadership in study start-up, site feasibility, ethics submissions, investigational product oversight, SAE reporting, and closeout management. With experience at ICON plc, IQVIA, and Tom Baker Cancer Centre, he combines regulatory rigor, cross-functional leadership, and patient-centered execution to deliver compliant, efficient, and high-quality clinical trial outcomes. In recognition of his dedication and impact in clinical research, Ahmad was also honored with the Citizenship Award from Tom Baker Cancer Centre.
The purpose of a monitor-based Clinical Research Organization, such as Clinara, is to ensure that clinical trials are conducted with the highest level of quality, safety, and regulatory compliance. It provides structured monitoring of clinical study sites to verify protocol adherence, ensure accurate data collection, and protect participant well-being. By maintaining consistent oversight throughout the trial process, Clinara helps generate reliable clinical evidence that supports medical innovation and regulatory approval.
From a monitor-based CRO perspective, Clinara views monitoring as a proactive and collaborative process rather than just an auditing function. Monitors serve as the bridge between sponsors and research sites, ensuring clear communication, identifying risks early, and supporting sites in maintaining compliance with study protocols. This perspective emphasizes precision, accountability, and partnership, ensuring that every clinical trial runs efficiently while maintaining patient safety and data integrity.
Clinara pledges to uphold the highest standards of ethical conduct, quality assurance, and regulatory compliance in every clinical study it supports. It is committed to safeguarding participant safety, ensuring the integrity of clinical data, and delivering transparent, consistent monitoring practices. Clinara also pledges to continuously improve its processes and support research teams in advancing safe, effective, and trustworthy clinical research outcomes.
Partnering with Clinara means choosing expertise, reliability, and a patient-first approach that drives successful clinical outcomes.
We use advanced risk-based strategies to identify issues early, prioritize critical data, and improve overall study efficiency.
We place research participants at the center of every study, ensuring safety, ethical practices, and a better trial experience.
Our skilled coordinators and clinical experts bring deep industry knowledge to manage trials efficiently and accurately.
With modern tools and dashboards, we provide continuous insights to detect risks, inconsistencies, and performance issues early.
We follow strict global standards and best practices to ensure every study meets or exceeds regulatory requirements.
Our streamlined processes reduce delays, optimize workflows, and help bring treatments to market faster.
We ensure accurate, consistent, and audit-ready data that supports successful regulatory submissions.
From early-phase trials to complex studies, our solutions are tailored to meet your specific needs.
Contact us now to explore how our Expert CRO Services can accelerate your research!
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