Iqvia Hiring for Clinical Research associate 2 Role

ByPharma Hiring Hub

IQVIA, a global leader in clinical research and healthcare intelligence, is hiring for the role of Clinical Research Associate II (CRA II) at its Ahmedabad location. This opportunity is suited for professionals with at least 1 year of on‑site monitoring experience and a Bachelor’s degree in Life Sciences who are looking to advance their career in clinical research and trial monitoring.

The role focuses on site monitoring activities, ensuring protocol compliance, data accuracy, and adherence to regulatory guidelines across clinical studies. Candidates will collaborate closely with investigators, site staff, and internal project teams to support high‑quality clinical trial execution.

This position offers strong exposure to global clinical trials, established monitoring practices, and long‑term career growth within a globally recognized CRO

Iqvia CRA2

Job Overview

  • Position: Clinical Research Associate 2
  • Department: CDM
  • Location: Ahmadabad, India(Home based)
  • Experience: 1+ Years
  • Qualification: B.Pharm
  • Job Type: Full-Time
  • Last Date to apply: 31 March 2026

Key Responsibilities – Clinical Research associate 2

  • Conduct site selection, initiation, routine monitoring, and close‑out visits in compliance with the contracted scope of work, GCP, and ICH guidelines.
  • Work closely with clinical sites to implement, monitor, and track recruitment plans, ensuring alignment with study timelines and enrollment targets.
  • Deliver protocol and study‑specific training to assigned sites and maintain regular communication to manage expectations and address ongoing issues.
  • Assess the quality and integrity of site practices, ensuring proper protocol conduct and regulatory compliance.
  • Identify and escalate quality issues as required.
  • Track study milestones including regulatory submissions and approvals, recruitment and enrollment, CRF completion, data query generation and resolution.
  • Support study start‑up activities when applicable.
  • Ensure essential site documents are available for filing in the Trial Master File (TMF).
  • Verify that the Investigator Site File (ISF) is maintained according to GCP and local regulatory requirements.
  • Prepare and maintain accurate monitoring visit reports, follow‑up letters, action plans, and other required study documentation.
  • Collaborate with study team members to support smooth project execution and timely issue resolution.
  • Support development of site‑specific recruitment plans.
  • Assist with site financial management, including tracking payments and retrieving invoices in line with local requirements and clinical trial agreements.

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.
  • Minimum of 1 year of on‑site clinical monitoring experience is required.
  • Good working knowledge of clinical research regulatory requirements, including GCP and ICH guidelines.
  • Therapeutic & Protocol Knowledge:Understanding of therapeutic areas and study protocols as provided through company training.
  • 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.
  • Organizational & Problem‑Solving Skills: Effective organizational, planning, and problem‑solving abilities to manage multiple study tasks.
  • Capable of managing time, priorities, and site‑level financial activities efficiently.
  • Ability to establish and maintain effective working relationships with study sites, coworkers, managers, and clients.

Why Join IQVIA?

  • Work on international studies across multiple therapeutic areas, collaborating with investigators, sites, and cross‑functional global teams.
  • Strengthen your expertise in ICH‑GCP compliance, protocol adherence, quality oversight, and inspection‑ready clinical trial conduct.
  • IQVIA promotes teamwork, continuous learning, and professional development through structured training, mentoring, and knowledge sharing.

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.

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FAQ-Clinical Research associate 2

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

Candidates with a Bachelor’s degree in Life Sciences or a healthcare discipline and at least 1 year of on‑site clinical monitoring experience.

2. What type of experience is required for this role?

Minimum 1 year of hands‑on on‑site monitoring experience, including activities such as site initiation, routine monitoring, and close‑out visits.

3. Is prior regulatory knowledge required?

Yes. A good working understanding of ICH‑GCP guidelines and global clinical research regulations is expected.

4. What will my main responsibilities be?

You will conduct site monitoring visits, ensure protocol and regulatory compliance, manage site documentation (TMF/ISF), support recruitment, and collaborate with study teams.

5. Will I work with investigators and site staff?

Yes. The role involves regular interaction with investigators, study coordinators, and site staff, including training and issue resolution.

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