Welcome To Clinnex
Clinnex is a contract research organization (CRO) dedicated to providing comprehensive clinical operations, biometrics, and technology services including:
- Clinical Operations
- Clinical Data Management
- Statistical Data Analysis
- Pharmacovigilance Services
- Clinical Data Standards
- Medical Writing & Consulting
- Remote Monitoring
- eTMF Services
to pharmaceutical, biotech, medical device companies and Clinical Research Organisations (CROs). With our focused delivery and technical capabilities, we are in an unparalleled position to meet both the regional and global needs of clients. We deliver quality outputs through the tireless efforts of our dedicated and ambitious workforce.
At Clinnex we believe in adopting proactive planning, maximizing output through innovation and technology, ensuring open communication, clear delineation of responsibilities and close collaboration with our clients.
Please feel free to browse our website which will provide you with useful information about our company and the services we have to offer.
We assist in binding clinical and biometric aspects of clinical trials to ensure clinical accuracy and integrity of trial data. With us specializing on biometrics services alone, we are well positioned to provide focused and responsive services.
Clinnex is a CRO providing Biometrics (Clinical Data Management, Statistical Data Analysis, Medical Writing and Consulting) services to Pharmaceutical, Bio-Tech, Medical Device Companies and Clinical Research Organisations (CROs).
Our detail oriented approach ensures embedding quality into all aspects of our deliverables. We take initiatives upfront to drive each task to successful completion and always look at ways to deliver tasks simpler, faster, precisely and with perfection.
Our Team
Sandeep Adsule
MANAGING DIRECTOR
Over 27 years of experience, across all phases of Clinical Trials and multiple therapeutic areas.
Successfully managed Asia-Pacific business, Singapore, Australia, New Zealand, South Korea, Taiwan, Thailand, Vietnam, China and Japan with Chiltern for more than 5 years.
Played vital roleĀ in setting up the relationship with 3 partner CROs in APAC. Set-up the PV Business Unit in India and achieved team size of 30 FTEs in a span of 1.5 years.
Thanuja Naidu
VICE PRESIDENT ā€“ BUSINESS OPS
Over 30 years of industry experience, including leadership of APAC clinical operations. Core expertise includes end-to-end clinical operations for the conduct of Phase Iā€“IV clinical trials, project management, and regulatory affairs, with proven country management experience within a multinational CRO environment.
Instrumental in establishing and scaling a Global Data Delivery Centre in India, driving operational excellence. Brings broad therapeutic experience including infectious diseases, oncology, rare diseases, and vaccines,. Has experience in managing MD and IVD trials, complex, global clinical development programs.
Dr. Ashoka K Singh
HEAD – MEDICAL
Over 30 years of industry experience including 25 years of experience in Clinical Research.
Worked in Major CROs in Clinical Operations and Medical Monitoring.
Expertise in Therapeutic areas such as Oncology, Psychiatry,Ā Infectious diseases etc.
Actively involved & has been part of Phase I to III trials and Patient based Pk Studies in different roles starting from CRC to VP Clinical Operations.
Kamakshi Sriram
HEAD – QUALITY ASSURANCE
A biochemist by qualification and is Q-IAOCR, ISO9001 certified Clinical Research Auditor.
Over 24 years of experience in scheduling, planning and conducting risk-based audits for Phase I to Phase IV site audits, vendor selection, GMP/GDP/GCP audits, CRO qualification, Central laboratory audits, Data base audits, eTMF/TMF (Medidata/Veeva) and Pharmacovigilance audits.Ā Conducted audits in more than 23 countries. Member of national and international societies on clinical research and Quality assuranceĀ .
Dr. Sarita Dimri
MEDICAL MONITOR
A medical and safety professional with over 18 years of multifaceted experience across dermatology, pharmacovigilance, clinical research, medical monitoring, and medical affairs.
Specialized in global safety management, including signal detection, risk mitigation, regulatory compliance, aggregate safety reporting, and clinical research support across diverse therapeutic areas.
Parvathi Chandrasekar
DIRECTOR – PROJECT MANAGEMENT
Over 23 years of work experience in the healthcare industry in India and US including 19 years in Clinical project & portfolio management. Experienced working with CRO, Pharmaceutical companies, academic & research organizations and NGOs.
By education, holds a Bachelor’s degree in Pharmacy and a Masters in Public health.
Experienced in managing large global studies across multiple therapeutic areas including Oncology (early drug Development), Neurology, Psychiatry, Cardiovascular and Infectious diseases across Preclinical, Phase 1, 2, 3 and 4 studies. Expert in managing multiple vendors, complex studies and cross functional teams.
David Ignatius
HEAD – BIOMETRICS
With over 30 years of experience in Clinical Data Management, Biostatistics and project management.
Worked with global contract research organizations (CROs) to successfully lead multiple complex studies.
Effectively managing resources and optimizing team performance while ensuring high-quality data collection and analysis.
Why Clients Love Us?
Why Choose Us
Clinnex strives to be a quality focused company, understanding the client requirements and the unique challenges in performing various types of clinical trials.
We work within a partnership model where our clients receive clear benefits from our domain expertise, project management experience, global reach, quality systems approach and multi-disciplinary data management capabilities.
Our Mission is to be acknowledged as a high quality Biometrics services provider and a preferred partner of our Clients by managing and accelerating biometrics deliverables more effectively to meet customer business goals.
