IQVIA Hiring – Clinical Research Associate I | Mumbai & Bangalore

ByPharma Hiring Hub

IQVIA, a global leader in clinical research and healthcare intelligence, is hiring for the role of Clinical Research Associate I (CRA I) at its Mumbai and Bangalore locations. This opportunity is suitable for B.Pharm and M.Pharm graduates with 0–3 years of experience who are looking to start or grow their career in clinical research and site monitoring.

The role focuses on supporting clinical trial monitoring activities, ensuring protocol compliance, data accuracy, and adherence to GCP and regulatory requirements. Candidates will work closely with investigational sites and cross‑functional project teams to support high‑quality clinical trial execution.

This is a strong entry‑level opportunity for professionals aiming to build a long‑term career in clinical research operations within a globally recognized CRO.

Iqvia CRA I opening

Job Overview

  • Position: Clinical Research Associate I
  • Department: CDM
  • Location: Bangalore, Mumbai
  • Experience: 0- 3 years
  • Qualification: B.Pharm, M.Pharm
  • Job Type: Full-Time
  • Last Date of application: 2 April 2026

Key Responsibilities – Clinical Research Associate I

  • Site Monitoring Activities: Conduct site selection, initiation, routine monitoring, and close‑out visits in line with the contracted scope of work and GCP / ICH guidelines.
  • Subject Recruitment Support: Work closely with investigational sites to implement, track, and drive subject recruitment plans, ensuring alignment with study timelines and project requirements.
  • Site Training & Communication: Deliver protocol and study‑related training to assigned sites.
  • Maintain regular communication with site personnel to manage expectations and resolve ongoing study issues.
  • Quality Oversight & Compliance: Evaluate the quality and integrity of site practices, ensuring proper protocol conduct and adherence to applicable regulatory requirements.
  • Identify and escalate quality issues to project teams as appropriate.
  • Study Progress Management: Monitor study progress by tracking regulatory submissions and approvals, recruitment and enrollment status, CRF completion, and data query generation and resolution.
  • Support study start‑up activities when required.
  • TMF & ISF Management: Ensure essential site documents (copies/originals as required) are available for filing in the Trial Master File (TMF).
  • Verify that the Investigator Site File (ISF) is maintained in compliance with GCP, ICH, and local regulatory requirements.
  • Monitoring Documentation: Create and maintain accurate monitoring visit reports, follow‑up letters, action plans, and other required site management documentation.
  • Cross‑Functional Collaboration: Collaborate with study team members to support timely and effective project execution.
  • Additional Study Responsibilities (If Applicable): Support the development of site‑specific subject recruitment plans.
  • Assist with site financial management, including tracking payments and retrieving invoices in accordance with executed clinical trial agreements and local requirements.

Required Skills & Qualifications

  • Bachelor’s degree in a scientific discipline or healthcare field is preferred.
  • An equivalent combination of education, training, and experience may be considered in place of a formal degree.
  • Some organizations may require completion of a CRA training program or prior monitoring experience.
  • Basic working knowledge of clinical research regulatory requirements, including GCP and ICH guidelines.
  • Good understanding of therapeutic areas and study protocols, as provided through company training programs.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.
  • Comfortable using laptops and mobile devices such as iPhone and iPad, where applicable.
  • Strong written and verbal communication skills, with a good command of the English language.
  • Effective organizational, planning, and problem‑solving abilities to manage multiple study activities.
  • Ability to manage time, priorities, and basic site‑level financial activities efficiently.
  • Ability to establish and maintain effective working relationships with investigators, site staff, coworkers, managers, and clients.

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 IQVIA website before applying.

Similar Job for fresher : Labcorp Hiring for Clinical Publishing Coordinator Role

FAQ – Clinical Research Associate I

1. Who can apply for the CRA I role at IQVIA?

Candidates with a Bachelor’s degree in Life Sciences, Pharmacy, or a healthcare‑related discipline, along with 0–3 years of experience in clinical research or monitoring, can apply.

2. Is this role suitable for freshers?

Yes. This role is suitable for freshers or early‑career professionals, especially those who have completed CRA training or have basic clinical research exposure.

3. What are the main responsibilities of a CRA I?

You will perform site monitoring visits, support subject recruitment, ensure protocol and regulatory compliance, manage study documentation (TMF/ISF), and collaborate with study teams for smooth trial execution.

4. Is prior monitoring experience required?

Prior on‑site monitoring experience is preferred but not always mandatory. Some candidates may qualify based on CRA training programs or relevant clinical research exposure.

5. What regulatory knowledge is required for this role?

A basic understanding of ICH‑GCP guidelines and clinical research regulations is expected. Additional training is provided by IQVIA.

Similar Posts