OUR COMPANY
Who We Are
ClinSite. a young and leading Site Management Organisation (SMO), provides a unified platform to sponsors, CROs and Clinical Trial Sites to effectively execute and obtain credible clinical trial data across multiple therapeutic areas.
Our project team have an exceptional clinical research experience, with an average of 10+ years in the industry across various therapeutic areas.
We appoint dedicated staff like CRCs, QA Executive, Site administration manager for each study to ensure centralized and smooth communications and quality work at site.
At ClinSite, we take each project as a chance to surpass expectations of our client, delivering solutions that not only meet objectives but also open new opportunities
What We Do
We work with Sponsors from pharmaceutical, biopharmaceutical, medical device companies, contract research organisations, academic research institutes and clinical research sites to make clinical trials available to patients.
Our network of sites has been built on relationships, past experience and knowledge of the sites’ capabilities.
ClinSite offers an end-to-end SMO service, standalone trial functions, or access to experienced clinical operations staff as needed, tailored to accommodate the specific needs of each client.
We advocate for a risk-based monitoring approach, enhancing the quality and effectiveness of clinical trials by assigning a dedicated project coordinator on site.
Why Partner with ClinSite
- Highly experienced team & health care providers
- Integrated clinical trial sites network
- Accurate and consistent documentation
- Expedited / fast pace regulatory approvals.
- Identify and enrol right participants into each study.
- Standardized SOPs for all sites
- Reducing workload for CRO, Sponsor and Clinical Trial Site
- Improve the quality of clinical trials.
- Support our partner in audit/regulatory inspection.
- Ensure the efficient and ethical conduct of trials.
- Cost effective
Network of Clinical Trial Sites
ClinSite has a integrated network of specialised and top enrollers – clinical trial sites (CTS) across various regions in the world. Our network sites have established the necessary infrastructure, human resources, and facilities to conduct research within these centres. All the sites are GCP-trained sites and strictly follow Good clinical practices that ensure the integrity and quality of the data produced in the clinical trials at optimal study speed.
Why choose ClinSite integrated network
- Access to large pool of participants
- Treatment-naïve patient populations
- Motivated Principal Investigators
- Proven track record
Our Solution for Sponsor, Site, CRO & Participant
Feasibilities
Through prequalified alliance site network
Quality Control
Through a qualified medical doctor for review and oversight at all network sites.
Regulatory Approvals
Through highly experienced professional ensuring expedited and fast pace approvals.
Quality Assurance
Through a seasoned professional having vast & international experience of internal and external audits.
Recruitment
Through collaboration with local community health centres, Government Institutes, doctors, clinics, and hospital database
Compliance
To study protocol through patient education, procedure for patient next visit reminders via dedicated follow-up team
Therapeutic Focus
ClinSite has sites and investigators working in the following clinical and therapeutic areas
Oncology
Immunology
Endocrinology
Infectious Disease & Vaccines
Gastroenterology
Dermatology
Nutrition
Cardiology
Pain Management
Anesthesia & Critical Care
Ophthalmology
Pulmonology
Gynaecology
Paediatrics
Surgery
Request for Proposal
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10+
Years of Research Experience
10+
30+
Sites in ClinSite Alliance Network
35000+
Participants Enrollement
80%
Exceed our Enrollment Goal
