If you are looking for a career in clinical research, site management, and clinical trial operations, this Clinical Research Coordinator (CRC) job in Mumbai at IQVIA is a strong opportunity. IQVIA is a global leader in clinical research and healthcare intelligence, known for high-quality trial execution and scientific excellence. This role is perfect for candidates with experience in clinical trials, patient management, documentation, and regulatory coordination.

Key Responsibilities

As a Clinical Research Coordinator, you will support end-to-end clinical trial activities, including:

• Conducting site and trial feasibility to identify qualified investigators.
• Compiling essential documents and assisting in regulatory submissions.
• Coordinating with site Ethics Committees for approvals and query resolution.
• Managing site setup, pre-screening, and review of patient databases.
• Handling clinical trial supplies – receipt, accountability, and storage.
• Preparing the site team for study initiation visits.
• Supporting the informed consent process and ensuring ethical compliance.
• Maintaining accurate and complete site documentation.
• Overseeing sample collection, lab logistics, and reviewing lab reports.
• Implementing patient recruitment strategies for timely enrollment.
• Ensuring CRF completion and resolving data queries within deadlines.
• Assisting monitors during monitoring visits and audits.
• Managing patient follow-ups, reimbursements, and payments.
• Handling drug accountability, storage, and dispensing documentation.
• Coordinating for site closeout and archival of essential documents.
• Maintaining study logs, manuals, and timely reporting to stakeholders.

Qualifications & Skills Required

• Bachelor’s/Master’s degree in Life Sciences, Pharmacy, Nursing, or related fields.
• Experience in clinical research, ICH-GCP guidelines, and site coordination preferred.
• Strong communication, patient interaction, and documentation skills.
• Ability to manage multiple tasks, timelines, and site operations efficiently.

Benefits of Working at IQVIA

• Opportunity to work with global clinical research leaders.
• Exposure to diverse therapeutic areas and large-scale clinical trials.
• Skill development in compliance, data management, and regulatory processes.
• Growth opportunities within clinical operations and project management.

How to Apply

Application Link