Experienced Data Review Associate – Hyderabad, India
Department: Data Management
Job ID: 11748
Location: Hyderabad, India
Company: Medpace – Global Clinical Research Organization (CRO)
Overview
Medpace, a leading global Clinical Research Organization (CRO), is expanding its footprint with the launch of a new office in Hyderabad, India. We are seeking an Experienced Data Review Associate to join our full-time Data Management team. This role offers the opportunity to contribute from the foundation stage and play an integral part in shaping operational excellence in a rapidly growing region.
As part of our strategic expansion, you will influence team development, cultural alignment, and cross-functional collaboration across global clinical research projects. This position is ideal for professionals seeking impactful work, long-term career advancement, and an opportunity to grow within a world-class CRO.
Why Join Medpace Hyderabad?
Foundational Role: Be among the first professionals establishing Medpace operations in Hyderabad.
High Impact: Use your expertise to drive operational success and regional growth.
Career Advancement: Expand into leadership roles as the Hyderabad office scales.
Global Collaboration: Work on advanced Phase I–IV clinical trials with international teams and reputable sponsors.
Strong Learning Culture: Medpace is recognized for stability, professional development, and long-term employee support.
Robust Infrastructure: Benefit from global systems, tools, and standardized processes of an established CRO.
If you are looking for a challenging, growth-oriented career and want to help build Medpace’s presence in India, this opportunity is designed for you.
Key Responsibilities
Conduct comprehensive manual reviews of clinical trial data.
Develop clinical review guidelines tailored to specific therapeutic areas.
Collaborate with the Data Management team to ensure timely query resolution.
Support data review activities across key therapeutic areas, including:
Oncology
Hematology
Infectious Diseases
Endocrinology
Metabolic Disorders
Qualifications and Experience Required
Bachelor’s degree in Nursing, Medicine, or an advanced clinical qualification.
Minimum 1–3 years of professional clinical or nursing experience, preferably in Oncology or Hematology.
Understanding of clinical trial processes and experience working with clinical data.
Working knowledge of MedDRA and WHO Drug dictionaries is an advantage.
Strong analytical, documentation, and data review skills.
About Medpace
Medpace is a global, full-service clinical contract research organization supporting the biotechnology, pharmaceutical, and medical device sectors. With more than 5,000 employees across 40+ countries and headquartered in Cincinnati, Ohio, Medpace drives the development of safe and effective medical treatments through scientifically grounded and disciplined operational excellence.
Our therapeutic expertise spans oncology, cardiology, metabolic diseases, endocrinology, central nervous system disorders, anti-viral studies, and infectious diseases.
Benefits at Medpace
Flexible working environment
Competitive compensation and benefits
Generous paid time-off packages
Structured career pathways with long-term growth potential
Employee appreciation programs
Health and wellness initiatives
Awards & Recognition:
Medpace has been named one of America's Most Successful Midsize Companies by Forbes for four consecutive years (2021–2024) and consistently receives CRO Leadership Awards for excellence in capability, reliability, and quality.
Next Steps
Once you submit your application, a Medpace recruitment team member will review your profile. Qualified candidates will be contacted with details on the interview and assessment process.
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