Experienced Data Review Associate – Hyderabad, India
Department: Data Management
Job ID: 11748
Work Model: Full-time, On-site
About the Role
A leading global Clinical Research Organization (CRO) is seeking an Experienced Data Review Associate to support the launch and growth of its newest office in Hyderabad, India. This is a strategic opportunity for experienced professionals who want to play a foundational role in building operations, shaping culture, and contributing to global clinical research excellence.
Experience Required
Minimum 2–5 years of experience in clinical data review, clinical research, clinical operations, or related healthcare domains.
Experience in oncology or hematology will be an added advantage.
Key Responsibilities
Conduct comprehensive manual review of clinical trial data for quality, accuracy, and adherence to study protocols.
Develop and maintain clinical review guidelines across targeted therapeutic areas.
Coordinate with Data Management teams to ensure timely resolution of data queries.
Contribute specialized expertise in one or more therapeutic areas, including:
Oncology
Hematology
Infectious Diseases
Endocrinology
Metabolic Disorders
Required Qualifications
Bachelor’s degree in Nursing, Medicine, or a related advanced clinical degree.
Professional or post-qualification nursing experience, preferably with oncology or hematology exposure.
Working knowledge of clinical trial processes and experience handling clinical data.
Familiarity with MedDRA and WHO Drug Dictionaries is advantageous.
Why This Role Is Unique
Founding Opportunity: Contribute to building and shaping the Hyderabad office from the ground up.
Immediate Impact: Your expertise will influence regional growth, team development, and operational excellence.
Global Exposure: Collaborate with international clinical teams and top-tier sponsors across multiple therapeutic areas.
Career Advancement: As the office expands, leadership and progression opportunities will grow with it.
Stable and Supportive Environment: Work within a global CRO known for disciplined processes, scientific expertise, and employee development.
About the Organization
This full-service CRO delivers Phase I–IV clinical development solutions to pharmaceutical, biotechnology, and medical device companies. With headquarters in Cincinnati, Ohio, and operations in 40+ countries, the organization brings strong scientific, therapeutic, and regulatory expertise across key areas such as oncology, cardiology, metabolic disease, endocrinology, CNS, antiviral, and anti-infective research.
Employee Benefits and Culture
Flexible work environment
Competitive compensation and benefits
Generous paid time off
Structured career paths for continuous growth
Employee appreciation programs
Health and wellness initiatives
Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024)
Recipient of multiple CRO Leadership Awards for quality, reliability, capability, and expertise
Join the Future of Clinical Research in Hyderabad
If you are an experienced clinical data professional seeking an opportunity to make a direct impact while advancing your career within a globally recognized CRO, this role offers the ideal platform. Apply today and contribute to building a strong foundation for future growth.
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Duluth | Eden Prairie | Fridley | Hibbing | Maple Grove | Minneapolis and St. Paul, Minnesota. | Minnetonka | St.Paul |Missouri :
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Galway |Meath :
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China | Quarry Bay |Hubei :
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Queensland |Remote Australia :
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Brussels |Flemish Brabant :
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Sofia |Canada :
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Australia | Mississauga | North York | Richmond Hill | Renfrew | Uxbridge |Quebec :
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Croatia |Zagreb :
Zagreb |Bohemia :
Prague |Republic of Egypt :
Cairo |Estonia :
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North Ostrobothnia :
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Jakarta |Israel :
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Auckland |Lima Region :
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Bucharest |Makkah :
Rabigh | King Abdullah Economic City | Khulais | Jeddah | Riyadh | Najran |Nišava District :
Niš |Singapore :
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Madrid |Sweden :
Sweden |Taipei :
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