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Eclinical Coordinator

Medpace
Medpace
1-2 years
Not Disclosed
Navi Mumbai, India
10 March 21, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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 – Clinical Data Management

Location: Navi Mumbai, India
Department: Data Management / eClinical
Employment Type: Full-Time (Office-Based)

Experience Required: 1–2 years (Freshers with strong fundamentals may also be considered)

Job Overview
We are hiring an eClinical Coordinator to support clinical data management and eClinical operations within a leading Contract Research Organization (CRO). This role is ideal for detail-oriented professionals who are passionate about clinical research and data accuracy. The position involves close collaboration with project managers and cross-functional teams to ensure high-quality data collection and reporting in clinical studies.

As part of the onboarding process, candidates will undergo structured training to develop expertise in eClinical systems, clinical trial workflows, and data management standards.

Key Responsibilities
Assist the eClinical Project Manager in system design, configuration, and study setup activities
Develop and maintain study-specific documentation in compliance with regulatory standards
Track study progress and generate key metrics to support project monitoring and reporting
Collaborate with clients and internal stakeholders to gather requirements and respond to queries
Ensure accuracy, consistency, and integrity of clinical data reported during studies
Support ongoing project activities and contribute to process improvements

Required Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related healthcare field
Strong attention to detail with a high level of accuracy
Working knowledge of Microsoft Excel and Word
Basic understanding of medical terminology

Preferred Skills and Experience
1–2 years of experience in a pharmaceutical company, CRO, or clinical research environment
Familiarity with clinical data management systems and eClinical platforms
Strong analytical, organizational, and communication skills
Ability to work in a structured, process-driven environment

Work Environment and Benefits
No travel required, office-based role in Navi Mumbai
Structured training and onboarding program for skill development
Opportunity to work on global clinical trials across multiple therapeutic areas
Clear career progression pathways within clinical data management and research operations
Supportive and collaborative work environment with a focus on professional growth

About the Organization
The hiring organization is a globally recognized Contract Research Organization (CRO) delivering Phase I–IV clinical development services to the pharmaceutical, biotechnology, and medical device industries. With a strong scientific and regulatory foundation, the organization is committed to accelerating the development of safe and effective therapies worldwide.

Why Apply
This role provides an excellent entry point into clinical research and eClinical data management, offering hands-on experience, global exposure, and long-term career growth in the life sciences industry.