Join IQVIA – Be at the Forefront of Healthcare Innovation!
Are you a Clinical Trial Assistant (CTA) or Clinical Trial Associate looking for an exciting opportunity in Mumbai? IQVIA is hiring a Clinical Process Associate with 1-3 years of experience in clinical research. This is a hybrid work role, offering flexibility and growth in a global leader in healthcare innovation.
Job Description: Clinical Process Associate
Key Responsibilities:
- Assist in clinical trial documentation and regulatory submissions.
- Support site management, investigator communications, and trial master file (TMF) maintenance.
- Coordinate with cross-functional teams to ensure smooth clinical trial operations.
- Ensure compliance with ICH-GCP guidelines and company SOPs.
- Track study progress, manage essential documents, and assist in clinical data review.
Qualifications & Skills:
- 1-3 years of experience as a Clinical Trial Associate (CTA), Clinical Trial Assistant, or similar role.
- Knowledge of clinical trial processes, ICH-GCP, and regulatory requirements.
- Strong organizational and communication skills.
- Proficiency in Microsoft Office & clinical trial software.
- Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field.
Why Join IQVIA?
IQVIA is a global leader in healthcare intelligence and clinical research, driving innovation to improve patient outcomes. With a strong presence in Mumbai and worldwide, IQVIA offers:
✅ Career growth in clinical research & healthcare.
✅ Hybrid work model for work-life balance.
✅ Competitive salary & benefits.
✅ Training & development in cutting-edge clinical trials.
How to Apply?
If you’re ready to take the next step in your clinical research career, send your updated resume to:
📧 Email: navitha.gouli@iqvia.com
📍 Location: Mumbai (Hybrid)
🔍 Job Reference: Clinical Process Associate – IQVIA Mumbai
