Medpace is a global, full-service clinical contract research organization (CRO) dedicated to advancing medical science and improving lives. With a rich legacy spanning over 30 years, Medpace specializes in providing Phase I-IV clinical development services to industries such as biotechnology, pharmaceuticals, and medical devices. Headquartered in Cincinnati, Ohio, we operate in more than 40 countries with over 5,000 employees worldwide.
Our core mission is to deliver safe and effective medical therapeutics through scientific expertise, disciplined processes, and a passion for innovation. Recognized by Forbes and Life Science Leader magazine, Medpace continues to lead the way in clinical research excellence.
Responsibilities in Job: What You’ll Do as a Data Review Associate
As a Data Review Associate at Medpace, you’ll be part of the Global Clinical Coding & Support team in Navi Mumbai. In this pivotal role, you will:
- Conduct Comprehensive Data Reviews: Perform detailed manual reviews of clinical trial data to ensure accuracy and compliance.
- Develop Clinical Review Guidelines: Create tailored review protocols for various therapeutic areas, including oncology, hematology, infectious diseases, endocrinology, and metabolic disorders.
- Collaborate with Data Management Teams: Work closely to resolve data queries efficiently and effectively.
- Specialize in Therapeutic Areas: Focus on key medical fields to ensure the highest quality clinical trial outcomes.
This role is integral to the success of Medpace’s global clinical trials and offers opportunities to grow and specialize in therapeutic areas of your interest.
Ideal candidates will possess:
- Attention to detail and strong analytical abilities.
- Effective communication skills to collaborate with global teams.
- A passion for clinical research and a commitment to improving patient outcomes.
- A proactive mindset and eagerness to develop within the therapeutic areas.
