Experienced Data Review Associate

Medpace, a rapidly growing global Clinical Research Organization (CRO), is excited to announce that we're looking for experienced full-time, Hyderabad-based Data Review Associate to join us as we prepare to launch of our newest office in Hyderabad, India.

This is more than just a job. It's an opportunity to be part of something from the very beginning. You'll play a direct role in shaping the culture, building the team, and influencing how we grow in India. From day one, your work will make a meaningful impact across global projects.

Why Join Medpace in Hyderabad?

• Be a Founding Member: Help establish and lead operations at our newest location.
• Immediate Impact: Your experience will directly influence Medpace's growth in the region.
• Career Growth: As the office grows, so will the leadership and advancement opportunities.
• Global Reach: Work on cutting-edge clinical trials with international teams and top-tier sponsors.
• Strong Culture: Join a company known for its stability and commitment to professional development.
• Support & Infrastructure: While the Hyderabad office is new, you'll be backed by the global resources and processes of a well-established CRO.

If you're looking for a new challenge, and want to be part of building something meaningful while advancing your career with a company that's investing in your region — we'd love to hear from you.

Help shape the future of Medpace in Hyderabad. Apply today.

• Comprehensive manual review of clinical data collected in trials
• Development of clinical review guidelines for specific therapeutic areas
• Interface with Data Management team to assure query resolution

• Seeking specialization in following therapeutic areas:

  • Oncology
  • Hematology
  • Infectious Disease
  • Endocrinology
  • Metabolic disorders

• Bachelor's Degree in Nursing / Medicine, or more advanced clinical degree 
• Professional / or Post-Qualification Nursing experience, preferably in Oncology and Hematology background
• General knowledge of clinical trial processes and/or experience working with clinical data
• Experience with using MedDRA and WHO Drug dictionaries will be a plus.

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment 
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.