Are you a graduate or postgraduate in Life Sciences looking to build a career in clinical research and centralized monitoring? IQVIA, a global leader in healthcare and clinical trials, is hiring a Centralized Monitoring Assistant in Kochi.
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This role is ideal for candidates with a keen eye for detail, knowledge of ICH-GCP guidelines, and a passion for supporting global clinical studies. If you’re ready to grow your career in one of the most in-demand fields in healthcare, this opportunity is for you.
Key Responsibilities
As a Centralized Monitoring Assistant, you will:
- Support centralized monitoring activities for ongoing clinical trials.
- Ensure compliance with ICH-GCP, local regulations, and company SOPs.
- Perform accurate data entry and maintain high-quality records.
- Communicate effectively with study teams, investigators, and site staff.
- Assist in generating reports, presentations, and documentation.
- Handle assigned tasks within given timelines to support trial deliverables.
Required Qualifications
To qualify for this role, candidates must have:
- Graduate/Postgraduate degree in Life Sciences or equivalent.
- Minimum 2 years of work experience, with at least 6 months relevant experience.
- Basic knowledge of research and regulatory requirements (ICH-GCP, local laws).
- Proficiency in Microsoft Word, Excel, PowerPoint.
- Excellent written and verbal communication skills in English.
- Strong time management, organizational, and data entry skills.
- Ability to work collaboratively with coworkers, managers, and clients.
Why Join IQVIA?
- Work with a global leader in healthcare research.
- Gain hands-on experience in centralized and risk-based monitoring.
- Competitive salary and benefits package.
- Exposure to international clinical research projects.
- Opportunities for career growth in one of the fastest-growing industries.
Application Process
Interested candidates can apply by sending their updated resume to:
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