IQVIA, a global leader in healthcare research and innovation, is hiring Clinical Research Associate-II (CRA-II) professionals across major metro cities in India. This role is ideal for candidates with proven onsite monitoring experience in clinical research who are ready to take the next step in their career.
If you are passionate about advancing clinical trials and improving patient outcomes, this is your chance to elevate your career with IQVIA.
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🔹 Job Responsibilities
As a CRA-II at IQVIA, you will:
- Conduct onsite monitoring visits and ensure compliance with study protocols.
- Perform 90+ interim monitoring visits to support ongoing clinical trials.
- Ensure adherence to GCP guidelines, SOPs, and regulatory requirements.
- Collaborate with investigators, site staff, and project teams to ensure smooth study execution.
- Identify, document, and resolve data discrepancies.
- Provide ongoing support to investigative sites and maintain quality documentation.
🔹 Qualifications
- Education: B.Pharm, M.Pharm, Pharm.D, BHMS, BAMS, or BDS.
- Experience: Minimum 2+ years of onsite monitoring in clinical research.
- Must have completed at least 90+ interim monitoring visits.
- Strong knowledge of ICH-GCP, clinical trial protocols, and regulatory requirements.
- Excellent communication and site management skills.
❌ Note: Freshers are not eligible for this role.
🔹 Benefits of Joining IQVIA
- Work with a global leader in healthcare research.
- Competitive salary and performance-based incentives.
- Professional growth and international exposure.
- Collaborative and inclusive workplace culture.
- Opportunity to contribute to cutting-edge clinical trials.
📌 How to Apply
Interested candidates can apply by sending their updated CV to:
📧 ashwini.veerabhadrappa@iqvia.com
👉 Apply soon to secure your spot with IQVIA India.
