Clinical Trial and Project Management
Full-Service Coordination of Clinical Research in Dermatology
At Maxeome, clinical trial and project management is handled to the highest standards in the industry. We deliver organized, reliable execution backed by deep expertise in dermatology and aesthetic medicine. Our approach is built on consistency, clear communication, and a strong understanding of site needs and sponsor expectations.
Our Experience in Clinical Trial Management
Maxeome brings extensive experience managing clinical trials within dermatology and aesthetic medicine, delivering consistent and reliable support throughout each study phase. Our team understands the complexities of multi-site trials and the importance of maintaining adherence to Good Clinical Practice (GCP) guidelines. We integrate operational agility with a clear understanding of regulatory requirements for studies to run smoothly, from site initiation through close-out.
With a strong network of dermatologists and clinical sites across Saudi Arabia, we ensure effective communication and coordination tailored to the unique requirements of each trial. Our approach prioritizes transparency, risk management, and effective execution.
What We Offer
Site Feasibility and Selection
Site Initiation and Training
Patient Recruitment and Retention
Study Logistics and Supply Management
Ongoing Site Support
Monitoring and Data Oversight
Regulatory Document Management
Project Management and Reporting
Streamlining Every Phase of Clinical Research
Our Capabilities
End-to-End Trial Management
We support your study from planning through execution by providing comprehensive services including site feasibility and selection, site activation and training, patient recruitment and retention strategies, study drug logistics and vendor coordination, and ongoing site communication and support.
Project Oversight and Coordination
Every project has a dedicated project manager responsible for site management, milestone tracking, budget and resource management, risk mitigation, regular status updates.
Documentation and Regulatory Compliance
We maintain full regulatory compliance documentation, including Trial Master File (TMF) setup and maintenance, site regulatory document collection, adverse events reporting, as well as Monitoring Visit Reports (MVRs).
Digital Infrastructure
We ensure efficient and secure data management through the use of electronic Case Report Forms (eCRFs), secure data capture with audit trails, remote and hybrid monitoring options, and collaboration-ready platforms for seamless interaction between sponsors and sites.
