IQVIA hiring Centralized Monitoring Assistant in Kochi. Apply now for clinical research jobs in life sciences, pharmacy, and healthcare.
Are you a graduate or postgraduate in life sciences, pharmacy, or clinical research and looking for an exciting career opportunity? IQVIA, a global leader in clinical research and healthcare intelligence, is inviting applications for the position of Centralized Monitoring Assistant in Kochi, Kerala.Centralized Monitoring Assistant Job
This role is best suited for professionals with at least 6 months to 2 years of clinical research experience who want to strengthen their career in centralized monitoring and clinical trial management.
Job Overview
- Position: Centralized Monitoring Assistant
- Company: IQVIA
- Location: Kochi, Kerala
- Qualification: B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences
- Experience: 6 months – 2 years in clinical research
- Application Mode: Email
- Status: Verified Job
About IQVIA
IQVIA is one of the world’s leading organizations in clinical trials, healthcare analytics, and technology-enabled solutions. With operations in over 100+ countries, IQVIA provides innovative approaches to research, drug development, and real-world evidence generation. Joining IQVIA means being part of a global team that works on cutting-edge healthcare solutions while supporting the advancement of clinical science. Centralized Monitoring Assistant Job
Key Responsibilities of Centralized Monitoring Assistant
As a Centralized Monitoring Assistant at IQVIA, you will be responsible for supporting clinical trial monitoring and ensuring that studies are conducted ethically, efficiently, and in compliance with global standards. Your responsibilities will include: Centralized Monitoring Assistant Job
- Supporting centralized monitoring activities for ongoing global clinical trials.
- Ensuring compliance with ICH-GCP guidelines, local regulatory requirements, and company SOPs.
- Performing accurate data entry and maintaining high-quality trial records.
- Communicating with study teams, investigators, and site staff for smooth trial operations.
- Preparing and assisting with reports, presentations, and clinical documentation.
- Managing assigned tasks within strict timelines to ensure trial deliverables are met.
Required Qualifications and Skills
To be successful in this role, candidates should meet the following requirements: Centralized Monitoring Assistant Job
- Graduate/Postgraduate degree in Life Sciences, Pharmacy, or equivalent.
- At least 6 months to 2 years of relevant experience in clinical research or centralized monitoring.
- Knowledge of ICH-GCP guidelines and local regulatory frameworks.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
- Strong written and verbal communication skills in English.
- Excellent organizational, documentation, and time management skills.
- Ability to work effectively with coworkers, managers, and clients in a collaborative environment.
Why Join IQVIA?
Working at IQVIA offers you the opportunity to grow in one of the fastest-growing industries in the world while being part of a global healthcare leader. Some benefits include: Centralized Monitoring Assistant Job
- Exposure to international clinical research projects.
- Hands-on experience in centralized and risk-based monitoring.
- Competitive salary and comprehensive benefits package.
- Work with a supportive team of experienced professionals.
- Strong career growth opportunities within the global IQVIA network.
How to Apply
If you are ready to take the next step in your clinical research career, apply for the Centralized Monitoring Assistant role at IQVIA by sending your updated resume to: Centralized Monitoring Assistant Job
📧 foram.chheda@iqvia.com
Subject Line: Application for Centralized Monitoring Assistant – Kochi
