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Medpace

Global CRO delivering full-service clinical trials

Data Coordinator - Entry

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeNavi Mumbai, Maharashtra, IndiaNo salary listed

About the Job

Requirements

  • A bachelor's degree in Life Sciences, Pharmacy, Health Sciences, or a related field is required.
  • 0–2 years of clinical data management experience is required.
  • Prior clinical research or site experience is required.
  • Proficiency in Excel is required.

Responsibilities

  • Monitor electronic data capture data quality, case report form completion, query, and source data verification metrics.
  • Perform clinical data review, cleaning, reconciliation, and discrepancy management.
  • Generate, review, and resolve data queries and programmed edit-check outputs.
  • Develop and maintain data management documents, specifications, and study plans.
  • Conduct user acceptance testing and validation of electronic data capture screens, edit checks, and external data processes.
  • Manage electronic data capture user access, system support, and training for study teams and sites.
  • Coordinate external data transfers, vendor reconciliation, and data-cleaning activities.
  • Prepare data metrics and reports to support study tracking and decision-making.
  • Collaborate with sponsors, vendors, and cross-functional teams to ensure timely data delivery.

Desired Qualifications

  • Mumbai candidates are preferred.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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