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Eclinical Coordinator

Medpace
Medpace
1-2 years
Not Disclosed
10 Jan. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

eClinical Coordinator – Data Management

Location: Navi Mumbai, Maharashtra, India
Department: Data Management / eClinical
Job ID: 12323
Experience Required: 1–2 years in pharmaceutical or CRO settings
Employment Type: Full-Time | Office-Based


Job Summary

We are seeking a detail-oriented eClinical Coordinator to join our Data Management / eClinical team in Navi Mumbai, India. The role involves supporting clinical study operations by ensuring the accuracy, integrity, and compliance of patient-reported data across clinical trials. Reporting to the eClinical Project Manager, the coordinator will contribute to study setup, documentation, monitoring, and client communications.

This position is ideal for candidates who thrive in a structured, standardized work environment, have strong organizational skills, and are eager to build expertise in clinical data management. All new hires undergo comprehensive onboarding and training to become proficient in eClinical processes and systems.


Key Responsibilities

  • Assist the Project Manager in the design, setup, and implementation of eClinical systems.

  • Prepare and maintain study-specific documents, templates, and tracking tools.

  • Monitor and report key study metrics, timelines, and project progress.

  • Collaborate with clients to gather requirements, respond to inquiries, and provide study updates.

  • Support ad hoc projects and tasks as assigned by the eClinical team.


Required Qualifications

  • Bachelor’s degree in a health-related field, life sciences, pharmacy, or equivalent.

  • 1–2 years of experience in a pharmaceutical, clinical research, or CRO environment preferred.

  • Strong working knowledge of Microsoft Excel, Word, and other office productivity tools.

  • Basic understanding of medical terminology and clinical trial documentation.

  • High attention to detail, accuracy, and ability to maintain compliance standards.

  • Travel: Not required.


Why Join Medpace?

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to pharmaceutical, biotechnology, and medical device industries globally. Our mission is to accelerate the development of safe and effective medical therapies through a scientific and disciplined approach, leveraging local regulatory and therapeutic expertise across oncology, cardiology, endocrinology, CNS, metabolic diseases, and infectious diseases.

What We Offer

  • Flexible work environment and structured career development paths.

  • Competitive salary, benefits, and PTO packages.

  • Company-sponsored employee recognition events.

  • Health, wellness, and professional growth initiatives.

Awards & Recognition

  • Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024).

  • Multiple CRO Leadership Awards from Life Science Leader magazine for quality, reliability, and expertise.


How to Apply

Qualified candidates will be reviewed by the Medpace recruitment team. If shortlisted, you will be contacted for the next steps in the hiring process.

Apply via Email:

  • careers@medpace.com