IQVIA is seeking a highly skilled Clinical Research Associate (CRA) to join its team! As a CRA, you’ll play a critical role in ensuring the success of clinical trials.
🔍 About the Role
As a Clinical Research Associate, you’ll play a vital role in ensuring the smooth conduct of clinical trials, maintaining data accuracy, and upholding the highest quality standards in compliance with regulatory requirements.
You’ll work closely with sponsors, investigators, and site teams — ensuring clinical research processes run seamlessly and ethically.
🎯 Key Responsibilities
Conduct onsite monitoring visits to ensure compliance with ICH-GCP guidelines and trial protocols
Monitor and verify data accuracy and quality
Collaborate with cross-functional teams to ensure timely study execution
Identify and mitigate risks related to clinical trials
Ensure documentation integrity and adherence to timelines
🎓 Eligibility Criteria
Education:
BPharm / MPharm / Pharm D / BHMS / BAMS / BDS
Experience:
Minimum 2+ years of onsite monitoring experience
At least 90+ onsite interim monitoring visits
Note: Freshers are not eligible for this position
🌟 Why Join IQVIA?
Work on complex, global clinical trials that make an impact
Join a collaborative and dynamic work environment
Gain access to career growth and professional development opportunities
Enjoy a competitive salary and benefits package
📍 Job Details
Job Title: Clinical Research Associate – II
Location: Any Metro City (India)
Job Type: Full-time
Industry: Clinical Research / Pharmaceuticals
📨 How to Apply
If you’re an experienced CRA ready for a new challenge, send your CV to:
📧 ashwini.veerabhadrappa@iqvia.com