Clinical Research Coordinator Job at IQVIA, Freshers & Experienced

Apply for Clinical Research Coordinator role in Mumbai for B.Pharm/M.Sc graduates. Full-time field-based position at IQVIA.

IQVIA is hiring a Clinical Research Coordinator (CRC) for a full-time, field-based position in Mumbai. This role supports end-to-end clinical trial activities, ensuring that investigative sites meet study, safety and regulatory expectations. It is suited for candidates with strong organizational skills and an interest in clinical operations.

Company Overview

IQVIA is a global leader in clinical research, healthcare analytics and real-world data solutions. The organization supports biopharmaceutical companies in advancing clinical development, improving patient outcomes and accelerating access to innovative therapies. With a broad operational network and deep scientific expertise, IQVIA remains one of the most trusted partners in clinical research worldwide.

Job Role & Responsibilities

The Clinical Research Coordinator will work directly with clinical trial sites to support operational execution. Responsibilities include:

• Conducting site and investigator feasibility assessments to identify suitable trial sites.
• Compiling essential documents, preparing regulatory submissions and responding to ethics committee queries.
• Coordinating site setup, reviewing patient databases and supporting pre-screening.
• Managing clinical trial supplies, including receipt, accountability and storage.
• Preparing site teams for initiation visits and working closely with monitors.
• Supporting informed consent administration and ensuring patients understand study requirements.
• Maintaining accurate and complete site documentation throughout the study.
• Managing lab sample logistics, reviewing lab reports and updating investigators.
• Implementing patient recruitment and referral activities to support enrollment.
• Ensuring timely CRF completion, query resolution and adherence to data timelines.
• Supporting monitoring visits and internal/external audits, ensuring timely closure of findings.
• Coordinating follow-up visits, patient reimbursements and site payments.
• Managing drug accountability, dispensing and documentation.
• Ensuring adherence to protocol, regulatory requirements and ethical guidelines.
• Maintaining study logs, manuals and assisting with site closeout and archival of documents.

Eligibility / Qualifications

• Bachelor’s or Master’s degree in Pharmacy, Life Sciences or related field.
• Strong understanding of clinical research operations (preferred).
• Ability to coordinate multiple site-level tasks with accuracy.
• Strong communication and documentation skills.
• Experience in patient coordination or site management is an advantage.

Location & Salary

• Location: Mumbai, India
• Work Type: Full-time, field-based
• Salary: As per company standards (not disclosed)

Application Process

Interested candidates can apply through the official IQVIA career portal:

👉 Apply Here: https://jobs.iqvia.com/en/jobs/R1503449-0

Ensure your resume highlights experience in clinical site coordination, documentation and trial support.

FAQs

1. Who can apply for the CRC role at IQVIA?
Candidates with a B.Pharm, M.Pharm, B.Sc or M.Sc in Life Sciences who have interest or experience in clinical research.

2. Is prior CRC experience mandatory?
No, but familiarity with clinical trial processes is preferred.

3. Is this a field-based position?
Yes, the role requires on-site coordination at assigned trial sites.

4. What skills are important for success in this role?
Strong communication, documentation accuracy, patient coordination, regulatory understanding and time management.

5. How do I apply?
Submit your application directly through the IQVIA link provided above.

Summary Table

Tagged as: Pharma Jobs in Mumbai