Experienced Data Review Associate

Job Summary 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 Responsibilities 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 Qualifications 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 Overview 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 Why Medpace 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