Clinical Research Coordinator Job Opportunity at IQVIA | Apply Now
IQVIA, a leading global provider of clinical research services and healthcare intelligence, is seeking a Clinical Research Coordinator job to join its team in Mumbai. This essential clinical research job focuses on managing site feasibility, regulatory submissions, and ensuring patient compliance throughout the study lifecycle, key responsibilities of the clinical research coordinator job. If you are detail-oriented and ready to accelerate the development of innovative medical treatments, this is a prime IQVIA vacancy to advance your career.
- Designation: Clinical Research Coordinator
- Location: Mumbai, India
About The Company
IQVIA is a global leader that creates intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Those interested in a clinical research coordinator job at the organization can expect a dynamic environment where employees contribute to global health progress.
Key Responsibilities
The Clinical Research Coordinator ensures the smooth, compliant operation of the clinical site, covering all phases from initiation to closeout.
- Site Setup & Feasibility: Conduct site/trial feasibility to identify & select the right site and investigator for the study. Ensure site setup according to protocol.
- Regulatory Compliance: Ensure timely compilation of all essential documents; assist with regulatory package preparation; ensure timely submission; follow up with the site EC to resolve any queries; and obtain approvals. Ensure adherence to protocol, regulatory, and ethical guidelines, which are essential tasks for any clinical research coordinator job.
- Patient Management: Review patient database & pre-screening, identify physician network. Assist in administering informed consent to potential subjects and in discussing the patient information sheet in detail. Ensure patient follow-up visits and visit compliance; manage patient-related reimbursement; manage site-related payments.
- Logistics & Monitoring: Coordinate receipt, accountability & storage of Clinical Trial Supplies. Coordinate lab sample collection and logistics; review lab reports and update the PI. Manage and refine practices for a clinical research coordinator job by coordinating the conduct of monitoring visits and audits (Internal or External).
- Data Integrity: Ensure CRF Completion and query resolution on specified timelines.
Essential Expertise
- Skills: Excellent attention to detail, strong organizational skills, and a comprehensive understanding of ICH-GCP guidelines.
- Soft Skills: Ability to coordinate effectively with the monitor, site staff, and regulatory bodies.
If you are passionate about the operational excellence required for a successful clinical research job and possess expertise in site management and regulatory documentation, this clinical research coordinator job at IQVIA is your next step. Ensure you submit your application immediately to take advantage of this IQVIA vacancy before the deadline of December 5, 2025.
