Our Services > Clinical Monitoring & Project Management Services

Tech Observer CRAs are experienced in numerous therapeutic areas across drug, biologic and device trials. All of our CRAs have state-of-the-art communications tools in place to provide timely and responsive communications, real-time data accessibility and centralized tracking and management of procedures.

At Tech Observer, all monitoring activities are conducted in accordance with ICH GCP compliance and data integrity during each site visit, consistently retrieving high quality, on-time data. Tech Observer’s Clinical monitoring team ensures the adherence with standard operating procedures (SOPs) and strives to promote positive personal relationships with a high level of trust and confidence with all our customers.

Tech Observer has gained extensive experience in the organization and management of local and global phase II-IV clinical trials. Clinical Project Management is the core of our services. We can manage all aspects of your clinical trial from the beginning up to the end or tailor our services to your specific needs.

Here, at Tech Observer, we work on the model of “Dedicated Project Management” expertise.Our Project Managers understand our clients' confidence on effective communication and quality.

Tech Observer can provide a full clinical monitoring support in US, Europe and APAC Region.

Our Clinical Monitoring Services Include

• Site Identification, Qualification and Initiation
• Subject Accrual/Retention Strategy Enhancement
• Regulatory Document Preparation and Collection
• Budget and Contract Negotiation
• Investigator Meeting Planning and Presentation
• Site Personnel Training
• Interim Site Monitoring
• Clinical Study Material Accountability
• Site Termination