Job Title
Data Coordinator – Core Laboratory
Company
Medpace
Location
Hyderabad, India
Department
Data Management / Core Laboratory
Job ID
11923
Role Overview
The Data Coordinator – Core Laboratory supports clinical trial data management activities within core laboratory operations. The role focuses on assisting with data validation, data transfers, query resolution, and maintenance of clinical study data to ensure accuracy, completeness, and regulatory compliance.
This position contributes to global clinical research projects by supporting data integrity and coordination between internal teams and external stakeholders.
Key Responsibilities
1. Core Laboratory Data Support
Assist in preparation of Core Lab Data Management documentation
Support data handling activities for clinical studies
Ensure proper documentation of data management processes
2. Data Validation & Quality Control
Perform validation of:
Data transfers
Edit programs
Support quality checks to ensure data accuracy and consistency
3. Data Cleaning & Query Management
Perform data cleanup activities, including:
Edit checks
Data reviews
Data corrections
Resolve data discrepancies and support query resolution
4. Data Transfer Management
Send data transfers to external stakeholders
Ensure timely and accurate transmission of clinical trial data
Maintain proper documentation of data transfer activities
Required Qualifications
Education
Bachelor’s degree in:
Life Sciences
Pharmacy
Health-related field
Experience
1–2 years of experience in:
Pharmaceutical industry OR
Clinical Research Organization (CRO)
Experience in data handling or clinical trial support preferred
Required Skills & Competencies
Technical Skills
Strong working knowledge of:
Microsoft Excel
Microsoft Word
Familiarity with clinical data processes and data management workflows
Analytical Skills
Strong attention to detail
Ability to identify and resolve data inconsistencies
Ability to work with structured clinical datasets
Communication & Collaboration
Ability to work with cross-functional teams
Coordination with internal and external stakeholders
Clear written and verbal communication skills
Work Style
Organized and process-oriented
Ability to manage multiple tasks efficiently
Ability to meet deadlines in a regulated environment
Preferred Attributes
Exposure to clinical trial data management environments
Familiarity with CRO or pharmaceutical workflows
Interest in clinical research operations and data quality assurance
Company Overview
Medpace is a global full-service Contract Research Organization (CRO) conducting Phase I–IV clinical trials across multiple therapeutic areas. The company focuses on delivering high-quality clinical development services to accelerate the development of safe and effective medical therapies.
Work Environment
Global clinical research environment
Data-driven and compliance-focused setting
Opportunity to contribute to new office setup in Hyderabad
Collaboration with international clinical trial teams
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