IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With a strong focus on innovation and data-driven insights, IQVIA helps biotech, pharmaceutical, and healthcare organizations accelerate clinical development and improve patient outcomes. The company is known for its robust compliance with Good Clinical Practices (GCP) and adherence to global regulatory standards.
Job Description
Role: Centralized Monitoring Assistant
Industry: Clinical Research / Contract Research
Employment Type: Full Time, Permanent
Location: Kochi & Ahmedabad (Hybrid – 3 days office, 2 days WFH)
Experience: 6 months to 3 years
Educational Qualification: Graduate/Post Graduate in Life Sciences (B.Sc, B.Pharma, BDS, M.Pharma, M.Sc)
Key Responsibilities:
- Complete role-specific training to support project execution.
- Assist in administrative tasks such as generating reports, maintaining study documents, and updating systems.
- Follow ICH-GCP guidelines and regulatory requirements.
- Perform delegated tasks under the supervision of the Centralized Monitoring Lead/Specialist.
- Maintain effective communication with team members and clients.
- Ensure compliance with project timelines and quality metrics.
Required Skills & Qualifications:
- Basic knowledge of GCP (Good Clinical Practices) and clinical research regulations.
- Proficiency in MS Office (Word, Excel, PowerPoint).
- Strong verbal and written communication skills in English.
- Good data entry and time management skills.
- Ability to work in a hybrid model (office + remote).
Why Join IQVIA?
- Work with a globally recognized leader in clinical research.
- Hybrid work model for better work-life balance.
- Opportunities for career growth in clinical monitoring and research.
- Exposure to cutting-edge clinical trials and regulatory compliance.
How to Apply?
Interested candidates with 0.6 to 3 years of experience in clinical research can apply
