IQVIA, a global leader in clinical research and healthcare solutions, is inviting applications for the role of Clinical Research Associate I/II. This opportunity is open across major metro cities in India.
If you are an experienced professional with 1–3 years of onsite monitoring experience, this is your chance to accelerate your career with one of the world’s top Contract Research Organizations (CROs).
Key Responsibilities
As a Clinical Research Associate at IQVIA, you will:
- Conduct onsite monitoring of clinical trials in compliance with ICH-GCP guidelines.
- Ensure protocol adherence and regulatory compliance across study sites.
- Review essential documents, source data, and case report forms (CRFs).
- Collaborate with investigators, site staff, and project teams.
- Identify, document, and resolve study-related issues.
- Maintain accurate study files and timely reporting.
Required Qualifications
To be considered for this role, you should have:
- 1–3 years of onsite monitoring experience (mandatory).
- A degree in Pharmacy, Life Sciences, or a related discipline.
- Strong knowledge of ICH-GCP guidelines and clinical trial regulations.
- Excellent communication and organizational skills.
- Ability to travel across assigned trial locations.
Note: Freshers will not be considered for this role.
Benefits of Working with IQVIA
- Opportunity to work with one of the world’s leading CROs.
- Exposure to global clinical trials and advanced research methodologies.
- Professional growth and structured career progression.
- Collaborative work culture with a focus on innovation.
How to Apply
If you meet the criteria, share your updated CV at:
📩 ashwini.veerabhadrappa@iqvia.com
