ONKlinical Research
Advancing Clinical Research Through Excellence and Innovation
About ONKlinical Research
ONKlinical Research LLC is a distinguished Site Management Organization (SMO) delivering comprehensive clinical research solutions across the United States. With our extensive investigator database and unwavering commitment to quality, we serve pharmaceutical companies, biotechnology firms, and Clinical Research Organizations (CROs) with excellence.
Our mission is to be the trusted resource of choice for our clients, facilitating seamless collaboration between sponsors and research sites. We prioritize Quality, Uniformity, Ethics, Safety, and Timeline (QUEST) in every trial, ensuring compliance with GCP and US-FDA requirements while maintaining the highest standards of clinical research.
Our Services
Pre-Study Site Preparation
Comprehensive site feasibility, selection, and assessment services, including essential document preparation, investigator briefing, and IRB submission management.
Site Initiation
Expert staffing with experienced Clinical Research Coordinators, complete IMP management, and efficient patient pre-identification and follow-up services.
Site Monitoring
Thorough patient follow-up, precise data collection, maintenance of site documents, and dedicated research site liaison services.
Our Therapeutic Area
- Cardiovascular
- Endocrinology
- Gastroenterology
- Respiratory Disorders
- Infectious Diseases
- Weight Management
- Neurology
- Pain Management
- Rheumatology
- Dermatology
- Ophthalmology
- Women’s Health
Our Strong Suit
In ONKlinical Research, services are custom-made to our clients’ need. We help them to simplify their process and broaden their geographic exposure. The following are our strong hold which assists in achieving our mission.
- Associations with experienced physicians and coordinators across USA, which is continuously expanding.
- Accelerated patient recruitment.
- Use of technology for Source Documentation and TMF management.
- Evaluation of site facility, resources, source documentation practices.
- Recognition and development of prospective Principal Investigators.
- Appointment of trained site staff.
- Meeting the project timelines for patient enrollment and data management matrices.
- Protocol compliance, patient follow-up, safety reporting, IP accountability, data collection, and compliance with ICH-GCP and applicable regulatory guidelines.
- Facilitate the monitoring visits by keeping all the essential and source documents up to date thereby reducing the monitoring time to an admirable extent.
- Internal pre audit Quality Assurance visit to site upon audit notification.
- Keeping investigator sites ‘audit ready’ at any time-point. Our Clinical Research Coordinators (CRCs) conduct prior preliminary site review to make sure all documentation is complete and accurate and this helps reduce the frequency of visits from the CRO/Sponsor.
Start Your Clinical Research Journey with Us
Get in Touch with Us Today
We’re here to help you streamline your clinical research process. Whether you’re a sponsor, a research site, or a potential patient, we’d love to hear from you. Contact us today to learn more about our services and how we can assist you.
You can reach us via email at manager@onklinicalresearch.com
Our working hours are Monday to Friday, 8 am to 5 pm. We look forward to hearing from you and assisting with your clinical research needs.
