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Clinical Research Coordinator I - India

IH – Remote (Ex-US India)Full-time$12–$122026-08-21 → 2026-10-08
Based in India

Core

Coordinate and execute clinical trial activities, participant recruitment, and data management to ensure protocol compliance and participant safety.

Role type

Clinical Research Coordinator I (CRC I)

Builds

Clinical research studies for sponsors in gastrointestinal, hepatology, obesity, and cardiology

Domain

Clinical research / Healthcare

Required skills

ICH-GCP guidelines, Indian clinical research regulations, clinical trial documentation, participant recruitment, data entry, source documentation, regulatory compliance, study supply management (via careerplan.io/jobs/4700896006-clinical-research-coordinator-i-india-at-iterativehealth)

Preferred skills

Centralized clinical operations experience, CTMS/EDC/eSource/EMR/EHR systems, multiple site management

Technologies

CTMS, EDC, eSource, EMR/EHR

Responsibilities

Coordinate participant visits and obtain informed consent; Process and ship laboratory specimens; Maintain source documentation and eCRFs; Enter data into EDC systems; Manage investigational product accountability; Support study startup and site activation; Prepare for sponsor monitoring visits and audits.

Seniority

Junior, hands-on IC