Experienced Data Review Associate – Clinical Data Management
Location: Pune, India
Job ID: 11330
Employment Type: Full-Time
Function: Data Management | Global Clinical Coding & Support
Industry: Clinical Research | CRO
About the Company
Medpace is a global, full-service Clinical Research Organization (CRO) providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals across 40+ countries and is recognized for its scientific rigor, regulatory expertise, and commitment to improving patient outcomes worldwide.
Role Overview
Medpace is seeking an Experienced Data Review Associate to join its Global Clinical Coding & Support team in Pune, India. This role is ideal for professionals with a clinical or nursing background who are looking to transition into clinical research data management while continuing to apply their therapeutic expertise.
The position plays a critical role in ensuring the accuracy, consistency, and clinical integrity of data collected in global clinical trials, particularly across complex therapeutic areas.
Key Responsibilities
Perform comprehensive manual review of clinical trial data to ensure accuracy, consistency, and medical relevance.
Develop and maintain clinical data review guidelines for assigned therapeutic areas.
Collaborate closely with Data Management teams to support timely and effective query resolution.
Apply clinical judgment to identify data trends, inconsistencies, and potential safety or efficacy signals.
Contribute to data quality initiatives supporting regulatory submissions and inspection readiness.
Develop subject matter expertise in one or more of the following therapeutic areas:
Oncology
Hematology
Infectious Diseases
Endocrinology
Metabolic Disorders
Required Qualifications & Experience
Education:
Bachelor’s degree in Nursing, Medicine, or a higher clinical degree (mandatory).
Experience:
Post-qualification professional nursing or clinical experience, preferably in Oncology or Hematology.
Prior exposure to clinical trials, clinical research, or clinical data review is highly desirable.
Technical Skills:
General understanding of clinical trial processes and clinical data standards.
Experience using MedDRA and WHO Drug dictionaries is an advantage.
Core Competencies:
Strong analytical and critical-thinking skills.
High attention to detail and data quality focus.
Ability to work collaboratively within cross-functional, global teams.
Why Join Medpace
Opportunity to leverage clinical expertise in a global clinical research environment.
Structured career paths with long-term professional growth opportunities.
Competitive compensation and comprehensive benefits package.
Flexible and supportive work environment.
Employee health and wellness initiatives.
Company-sponsored employee engagement and appreciation programs.
Recognition & Awards
Named by Forbes as one of America’s Most Successful Midsize Companies (2021–2024).
Consistently recognized with CRO Leadership Awards by Life Science Leader magazine for expertise, quality, reliability, and capabilities.
What Happens Next
Qualified candidates will have their profiles reviewed by the Medpace recruitment team. Selected applicants will be contacted with details regarding the next steps in the hiring process.
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