eClinical Coordinator – Data Management / eClinical
Location: Navi Mumbai, India
Department: Data Management – eClinical
Job ID: 12323
Employment Type: Full-Time, Office-Based
Travel Requirement: None
About the Role
ThePharmaDaily.com is hiring for the position of eClinical Coordinator in Navi Mumbai, India. This full-time, office-based opportunity is ideal for candidates seeking to build a career in clinical data management, electronic clinical systems (eClinical), and patient-reported outcomes (ePRO) within a global Clinical Research Organization (CRO) environment.
As an eClinical Coordinator, you will collaborate closely with the eClinical Project Manager and cross-functional clinical trial teams to ensure accurate collection, validation, and monitoring of patient-reported and site-reported clinical trial data. This role offers structured onboarding and comprehensive training to develop technical expertise in clinical systems, trial documentation, and project tracking.
Key Responsibilities
Support the eClinical Project Manager in system design, configuration, and study set-up
Assist in the implementation and maintenance of eClinical platforms and electronic data capture (EDC) systems
Develop and maintain study-specific documentation and system-related materials
Track, analyze, and report key study metrics for effective project monitoring
Collaborate with sponsors and internal stakeholders to gather requirements and respond to project-related inquiries
Contribute to assigned clinical system and data management projects
Eligibility & Qualifications
Bachelor’s degree in a health-related field (Life Sciences, Pharmacy, Biotechnology, Nursing, or equivalent)
Strong attention to detail and analytical skills
Working knowledge of Microsoft Excel and Word
Knowledge of medical terminology
Excellent documentation and communication abilities
Experience Required
1–2 years of experience in a pharmaceutical company, biotechnology firm, or Clinical Research Organization (CRO) preferred
Fresh graduates with strong academic credentials and relevant internships may also be considered
About Medpace
Medpace is a global full-service Clinical Contract Research Organization (CRO) delivering Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, and operating across 40+ countries, the organization employs more than 5,000 professionals worldwide.
The company supports diverse therapeutic areas including oncology, cardiology, metabolic diseases, endocrinology, central nervous system disorders, anti-viral, and anti-infective research. With a scientific and disciplined operational model, Medpace accelerates the development of safe and effective medical therapies globally.
Why Consider This Opportunity?
Structured onboarding and domain-specific training in eClinical systems
Clear career progression in clinical data management and clinical trial technology
Competitive compensation and benefits package
Flexible and standardized work environment
Employee wellness initiatives and recognition programs
Industry Recognition
The organization has been recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024) and has received multiple CRO Leadership Awards for excellence in expertise, quality, reliability, and compatibility.
Application Process
Applications will be reviewed by the recruitment team. Shortlisted candidates will be contacted for further evaluation and next steps in the hiring process.
This role is ideal for professionals aiming to advance their careers in eClinical operations, electronic data capture systems, and global clinical trial support within the pharmaceutical and biotechnology sector.
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
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