IQVIA Hiring – Clinical Research Coordinator | Bangalore

ByPharma Hiring Hub

IQVIA, a global leader in clinical research and healthcare intelligence, is hiring for the role of Clinical Research Coordinator at its Bangalore location. This opportunity is suitable for B.Pharm and M.Pharm professionals with 3+ years of experience who are looking to advance their career in clinical research coordination and trial operations.

The role focuses on supporting study coordination activities, site and project support, documentation management, and coordination with cross‑functional teams to ensure smooth execution of clinical trials. Candidates will work within a regulated environment, supporting study timelines, compliance, and data quality.

This position offers strong exposure to global clinical trials, collaborative project teams, and long‑term career growth within IQVIA’s clinical research operations.

Iqvia-Career-crc

Job Overview

  • Position: Clinical Research Coordinator
  • Department: Clinical research
  • Location: Bengaluru, India
  • Experience: 3+ Years
  • Qualification: B.Pharm, M.pharm
  • Job Type: Full-Time
  • Last Date to apply: 4 April 2026

Key Responsibilities – Clinical Research Coordinator at iqvia

  • Assist with study data quality checks and support query resolution to ensure accurate and complete clinical data.
  • Perform a range of clinical research procedures, including ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and cardiac telemetry monitoring as per study protocol.
  • Record, report, and interpret study findings accurately to support the development and maintenance of a study‑specific database.
  • Assist investigators in ensuring study objectives are met on time, within budget, and in compliance with protocol requirements, regulatory standards, and quality expectations.
  • Provide training to new investigator site staff on study‑specific requirements.
  • Audit, maintain, and track site staff training records to ensure continued compliance.
  • Prepare for and participate in study monitoring visits, audits, and regulatory inspections, supporting interactions with clinical research regulatory authorities.
  • Assist research sites with staffing coverage planning and scheduling to support ongoing research activities.
  • Provide day‑to‑day clinical research support to investigators during study preparation and execution, including:

Required Skills & Qualifications

  • Bachelor’s degree is required
    OR
  • High School Diploma or equivalent, along with relevant experience.
  • Minimum 3 years of relevant work experience in a clinical or medical setting, such as:
    • Medical Assistant
    • Assistant Nurse
    • Laboratory Technician
  • An equivalent combination of education, training, and experience may also be considered.
  • Working knowledge of clinical trial conduct and Good Clinical Practice (GCP) principles.
  • Strong understanding of protocols, study‑specific operating procedures, informed consent forms, and study schedules.
  • Proven ability to perform required clinical procedures, including:
    • Intravenous catheter insertion
    • Spirometry testing
  • Proficiency in MS Windows and Microsoft Office applications, including Word, Outlook, and Access.
  • Excellent interpersonal and communication skills.
  • Strong attention to detail when performing clinical and documentation tasks.
  • Ability to establish and maintain effective working relationships with coworkers, managers, investigators, and clients.
  • Possession of applicable certifications or licenses, as required by company policies and relevant regulatory authorities at the country, state, or local level.

Why Join IQVIA?

  • Join IQVIA, a world‑leading organization in clinical research and healthcare intelligence, supporting global pharmaceutical and biotechnology companies.
  • The Clinical Research Coordinator role provides an opportunity to advance your career through hands‑on involvement in clinical trials, site coordination, and study operations.
  • Work on international clinical trials, gaining experience across study execution, regulatory compliance, and data quality processes.
  • Strengthen your expertise in Good Clinical Practice (GCP), protocol adherence, and regulatory standards within a highly compliant research setting.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.

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FAQ-Clinical Research Coordinator at iqvia

1. Who can apply for the Clinical Research Coordinator role at IQVIA?

Candidates with a Bachelor’s degree (or High School Diploma with relevant experience) and 3+ years of experience in a clinical or medical environment can apply.

2. Is this role suitable for experienced professionals?

Yes. This role is intended for professionals with prior experience in clinical research, clinical environments, or medical settings who want to advance into study coordination roles.

3. What are the main responsibilities of this role?

You will support clinical trial execution, perform clinical procedures, manage study documentation, assist investigators, coordinate site activities, and ensure GCP‑compliant study conduct

4. Does this role involve performing clinical procedures?

Yes. The role includes clinical procedures such as ECG, sample collection, spirometry, IV catheter insertion, vital signs, and study‑specific assessments.

5. Will I support subject recruitment and screening?

Yes. You will assist with patient recruitment, screening, informed consent support, subject orientation, and maintenance of screening logs.

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