Welcome to UNICO Clinical Research Services
Ethical & Reputed
Site Management
Organization (SMO)
|
Who We Are
Established in 2023, Unico Clinical Research Services (UCRS) is a leading Site Management Organization dedicated to supporting clinical research through comprehensive site management services.
We operate across multiple sites in India, including Delhi NCR, ensuring high-quality research, ethical conduct, and regulatory compliance.
Our Mission
To accelerate clinical research by delivering high-quality, ethical, and patient-centered site management solutions.
Our Vision
To become a global leader in clinical trial site management, driving innovation and advancing healthcare through clinical research.
Bio Specimens
We are collecting Bio Specimens in all Therapeutic areas.
Our Role in Clinical Research
As a Site Management Organization, we act as a bridge between Sponsors, CROs, Investigators, and Research Sites.
- Identifying and managing high-performing research sites
- Ensuring regulatory and ethical compliance
- Streamlining patient recruitment and retention strategies
- Coordinating clinical trial activities
- Ensuring accurate and timely data collection
- Supporting investigators and research teams throughout the study
Built for Clinical Excellence
Ethical Conduct
Committed to GCP, ICH guidelines, and the highest standards of patient safety and data integrity.
Strong Site Network
Access to a robust network of qualified research sites and experienced investigators across India.
Timely Delivery
Proven track record of on-time trial start-up, enrollment, and study close-out across all phases.
Regulatory Expertise
Deep understanding of CDSCO, IRB/EC processes, and documentation requirements for Indian clinical trials.
Your Trusted SMO Partner
Experienced Team
Our clinical operations team brings hands-on experience across all phases of clinical trials.
Multi-Therapeutic Expertise
We operate across oncology, cardiology, CNS, infectious diseases, and many more therapeutic areas.
Patient-Centric Approach
Recruitment and retention strategies designed to prioritize patient experience and study compliance.
End-to-End Support
From site identification and regulatory submissions to data collection and study close-out.
Therapeutic Areas We Cover
Comprehensive Clinical Site Management Services
Empowering your trials from initiation to submission with end-to-end solutions.
Site Identification & Feasibility
Evaluating potential sites based on investigator expertise, patient population, and study requirements to ensure optimal trial execution.
Regulatory Support
Managing IRB/EC submissions, SAE/SUSAR notifications, and annual regulatory reports with strict adherence to global standards.
Specialized Site Support
Rapid site start-up, patient recruitment & retention, and end-to-end coordination to keep your trial on schedule.
Training & Team Development
GCP-compliant training programs for investigators, study coordinators, and site staff to maintain quality and compliance.
Clinical Operations
Overseeing trial progress monitoring, protocol adherence, data quality, and compliance across all study phases.
Feasibility Assessment
In-depth evaluation of site capabilities, patient availability, investigator experience, and operational efficiency.
Career Opportunities
Join our growing team of clinical research professionals. We welcome passionate individuals interested in advancing medical research.
- Ethical and compliant work environment
- Exposure to diverse therapeutic areas and clinical trials
- Work closely with investigators, sponsors, and CROs
- Be part of a growing Site Management Organization
- Contribute to advancing medical research across India
Ready to Join Us?
Send us your resume and tell us about yourself. We'll get back to you as soon as a suitable opportunity arises.
Send Your ResumeOpens your email app directly
Get In Touch
Have a question or want to work with us? We'd love to hear from you.
Address
117, Deena Garhi, Lohia Nagar,
Main Road, Ghaziabad 201001
Phone
+91 79826 72370