Are you detail-oriented, organised, and eager to grow in the clinical research industry? If yes, an exciting opportunity awaits you in Noida! This Centralised Monitoring Assistant role offers the perfect blend of administrative responsibility, data oversight, and project coordination—all within a leading global healthcare environment.
📝 About the Role
As a Centralised Monitoring Assistant, you’ll be an essential part of the clinical study management team. Your role ensures that clinical projects run smoothly and efficiently. Here’s what you’ll be doing:
✨ Administrative Support: Assist clinical study teams with essential study-level administrative tasks.
🖥️ System Updates: Maintain and update systems as per project timelines and requirements.
🔐 Access Management: Perform vital access-related administrative tasks to support ongoing studies.
📊 Data Review: Evaluate site-level KRIs and historical site performance as outlined in the Central Monitoring Plan.
📚 Eligibility & Requirements
To excel in this role, you’ll need:
🎓 Education: Graduate/Postgraduate in Life Sciences or an equivalent field.
💼 Experience: At least 2 years of work experience, including a minimum of 6 months of relevant experience.
🛠️ Skills:
- Basic knowledge of clinical research and regulatory requirements
- Proficiency in Microsoft applications
- Strong written and verbal communication skills
🌈 What You Can Expect
Joining this role means stepping into an environment where learning and growth never stop:
🚀 Career Growth: Accelerate your career in an industry with immense global impact.
🤝 Collaborative Culture: Work with experienced professionals driven by excellence.
💼 Competitive Benefits: Enjoy a competitive salary and employee benefits.
📧 How to Apply
Interested in advancing your career in clinical research? Apply now through the link below:
👉 Apply Here: https://jobs.iqvia.com/job/-/-/24443/88528553472?source=LinkedIn_Slots&utm_source=linkedin.com&utm_medium=job_posting
📘 Tips to Excel as a Centralised Monitoring Assistant
🗂️ Stay Organised: Manage multiple projects and deadlines effectively.
🗣️ Enhance Communication: Improve written and verbal communication for better coordination.
📖 Stay Updated: Keep learning about the latest trends in clinical research and data monitoring.
🤔 Why Choose This Role?
🏢 Work with an industry-leading clinical research organisation
🎯 Access training, upskilling, and professional development opportunities
👥 Collaborate with passionate experts in a dynamic and supportive environment