IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services to the life sciences industry. With a strong reputation for innovation and excellence, IQVIA has earned 3.94 out of 5 stars from over 156 reviews, reflecting its commitment to quality and employee satisfaction. The company operates in more than 100 countries, helping biotech, pharmaceutical, and medical device companies transform their clinical development and commercialization processes.
Job Description
IQVIA is hiring for the role of Centralized Monitoring Assistant in Kochi. This is an excellent opportunity for graduates or postgraduates in Life Sciences with 1-3 years of experience in clinical research. The role involves providing administrative support to clinical study management, assisting in project tracking, and monitoring site performance to ensure compliance with regulatory requirements.
Key Responsibilities
- Provide project-related assistance to assigned teams, ensuring adherence to standard operating procedures, good clinical practices, and regulatory requirements.
- Perform study-level administrative tasks such as preparing status reports, maintaining study trackers, and following up on outstanding issues.
- Assist in updating and maintaining systems within project timelines to ensure credible data for analysis.
- Support Central Monitors (CMs) in preparing i-site packs for assigned studies by pulling relevant reports.
- Perform access management-related administrative tasks, including processing access requests and coordinating with vendors.
- Assist Technical Solution Specialists (TSS) with Excel formulations and front-end tasks.
- Monitor site performance, identify risks, and recommend corrective actions such as Site Telephone Contact or Triggered Onsite Monitoring Visits.
- Attend Kick-Off meetings, weekly team meetings, and client meetings as required.
- Adhere to key activities outlined in the Statement of Work (SOW) as per customer requirements.
Qualifications
- Graduate or Postgraduate in Life Sciences or equivalent.
- Minimum of 2 years of work experience, with at least 6 months of relevant experience in clinical research.
- Basic knowledge of regulatory requirements, including ICH-GCP and local guidelines.
- Proficiency in Microsoft Office applications (Word, Excel, PowerPoint).
- Strong written and verbal communication skills in English.
- Effective time management and detail-oriented approach.
- Ability to build and maintain relationships with coworkers, managers, and clients.
- Good data entry and listening skills.
Why Join IQVIA?
- Work with a globally recognized leader in life sciences and healthcare.
- Gain exposure to cutting-edge technologies and innovative solutions.
- Be part of a collaborative and supportive work environment.
- Opportunities for professional growth and development.
How to Apply
