About ClinSite
ClinSite, a full-service Contract Research Organization (CRO), was founded by seasoned professionals with extensive experience and expertise in clinical research, healthcare, and pharmaceuticals. Our hands-on experience in overseeing end-to-end clinical studies across various therapeutic areas for international multicentre research has led to the inception of ClinSite.
We strictly adhere to national and international regulatory standards, ensuring compliance with ethical practices and relevant guidelines.
ClinSite provides invaluable assistance to principal investigators and sponsors, supporting them in conducting & managing clinical trial projects across various therapeutic areas and Phase I-IV clinical trials for pharmaceuticals, biopharmaceuticals, medical devices, and health-related products within a framework of competitive budgets and efficient execution methodology.
Our Vision
To become your trusted global partner in clinical trial management by delivering highest quality services across all clinical research activities. Through our unwavering dedication, we strive to make a difference in patients’ lives and contribute to global public health initiatives worldwide.
Our Mission
We aim to provide our in-depth expertise and therapeutic experience for your study success from the beginning to end.
OUR VALUES
Quality & Compliance
We ensure the quality and accuracy of research data, while adhering to regulatory and industry standards.
Passion & Integrity
We are excited about what we do and maintain unwavering integrity in all endeavours
Service
We deliver timely results and quality data
Freedom
We highly regard our ability to be flexible and autonomous
Responsibility
We keep promises
Client Focus
We meet and exceed client expectations
Strong Relationship
We build long-term partnerships built on trust
Leadership Team
DR. ROOH UL ARIFEEN
![roohularifeenprofile1](http://clinsite.org/wp-content/uploads/2024/05/roohularifeenprofile1.jpg)
Chief Executive Officer
ASIM MUNIR
![Asimmunirprofile](http://clinsite.org/wp-content/uploads/2024/05/Asimmunirprofile.jpg)
Head of Clinical Operations & Regulatory Affairs
MADNEE FAISAL
![madnee](http://clinsite.org/wp-content/uploads/2024/05/madnee.jpg)
Human Resource Manager
HAMZA SETHI
![HamzaSethi](http://clinsite.org/wp-content/uploads/2024/05/HamzaSethi.png)
Regulatory Affairs Manager
WALEED PERVAIZ
![WaleedPervaiz](http://clinsite.org/wp-content/uploads/2024/05/WaleedPervaiz.png)
Business Manager
Rija Ali Zaidi
![rija](http://clinsite.org/wp-content/uploads/2025/01/rija.jpg)
Business Development Manager
NOOR ALI
![noorali](http://clinsite.org/wp-content/uploads/2025/01/noorali.jpg)
Manager Business Operations
![roohularifeenprofile](http://clinsite.org/wp-content/uploads/2024/05/roohularifeenprofile.jpg)
Dr. Syed Rooh Ul Arifeen Naqvi
Chief Executive Officer
Dr. Syed is a seasoned healthcare provider and clinical research expert with over 8 years of experience in the healthcare sector. He holds a Bachelour of Medicine, Bachelor of Surgery (MBBS) degree from the University of Health Sciences and is certified as a Medical Doctor, ICH-GCP trained clinical research professional, and possesses Basic Life Support certification.
His career journey began as a Medical Officer at WilCare, where he advanced to the position of Senior Medical Officer. During his tenure, he established both the clinical trial site and the Bio-availability and Bio-equivalence centre at Olive Biocentre, a project under WilCare. Subsequently, he transitioned to Aga Khan University Hospital (AKUH), Pakistan’s largest and premier clinical trial site, as a Senior Medical Officer.
Driven by his passion for clinical research, Dr. Syed joined DRK Pharma Solutions GmbH as Lead Commercial and Operations, where he rapidly ascended to the role of Clinical Research Project Lead. In this capacity, he oversaw global multi-centric clinical trials, spearheading the planning, execution, and delivery of numerous biosimilars, prophylactic vaccines, and therapeutic trials, including those in the realms of vaccines and oncology. From negotiating budgets to overseeing study startup, maintenance, and site closeout activities, he ensured strict adherence to Good Clinical Practice (ICH-GCP) guidelines and regulatory requirements. Moreover, Dr. Syed actively contributed to the business development and communication strategies of the company, leveraging his adeptness in social media marketing and extensive industry network.
As part of his commitment to community service, Dr. Syed is associated with an Islamabad based NGO that offers healthcare services to marginalized populations.
![Asimmunirprofile](http://clinsite.org/wp-content/uploads/2024/05/Asimmunirprofile.jpg)
Asim Munir
Head of Clinical Operations & Regulatory Affairs
Over the past 8+ years, Mr. Asim has specialized in clinical research, with expertise in clinical operations, project management, regulatory affairs, business development, and commercialization. His most recent role was as General Manager – Commercial & Operations and Head of Regulatory Affairs at a Swiss-headquartered Contract Research Organization (CRO).
Certified in clinical research by the National Institute of Drug Abuse and the National Institute of Health, USA, Mr. Asim has managed Phase II and Phase III multi-regional clinical trials in oncology, rabies, polio, and COVID-19 vaccines. He played a pivotal role in the expansion of CRO services to Bangladesh, Nepal, and Sri Lanka and demonstrated exemplary leadership during the pandemic by successfully leading COVID-19 clinical trials.
Mr. Asim has held various positions in prominent pharmaceutical companies, including Business Unit Head for International Business Development, where he oversaw operations in the Philippines, Vietnam, Cambodia, Sri Lanka, the Maldives, Myanmar, and CIS countries. He has a track record of generating cross-border business, enhancing profitability, and driving productivity.
His experience also includes out-licensing of product development services (lab-scale development to finished pharmaceutical product supplies) to the renowned pharmaceutical companies in Europe and South Asia. He successfully sourced and managed a wide network of contract manufacturing organizations (CMO) and executed its services to international pharmaceutical companies who do not have their own manufacturing facility.
Team Experience
Our team With over 10 years of experience and proven track record of handling and managing end-to-end Phase II-IV clinical trials across diverse therapeutic segments, our team work closely with clients to provide tailored, flexible solutions that meet key milestones on time and within budget.
Oncology Projects
Infectious Disease Projects
Endocrinology Projects
Immunization Projects Experience
Pediatrics Disease Projects
10+
Years of Research Experience
10+
30+
Sites in ClinSite Alliance Network
35000+
Participants Enrollement
80%
Exceed our Enrollment Goal
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