Are you a life sciences graduate or post-graduate with 2-5 years of experience in clinical research? IQVIA, a global leader in healthcare and pharmaceutical services, is hiring for the role of Centralized Site Associate in Mumbai and Bengaluru. This is an excellent opportunity to work with a reputed organization and contribute to groundbreaking clinical trials. Read on to learn more about the job details, responsibilities, qualifications, and how to apply.
Job Overview
As a Centralized Site Associate at IQVIA, you will provide project-related assistance to clinical study management teams. Your primary responsibility will be to ensure all work is conducted in compliance with standard operating procedures (SOPs), good clinical practices (GCP), and regulatory requirements. You will play a crucial role in maintaining the quality and integrity of clinical trial data while meeting project timelines.
Key Responsibilities
- Provide administrative support to clinical study management teams, including preparing status reports, maintaining study trackers, and following up on outstanding issues.
- Perform centralized monitoring activities to evaluate site quality and protocol compliance.
- Prepare i-site packs for assigned studies and ensure data accuracy.
- Interact with sites and CRAs to resolve missing data, pending queries, and SDV backlogs.
- Conduct subject-level data reviews to ensure compliance with inclusion/exclusion criteria, IP, AE, labs, and endpoints.
- Assist in risk identification and recommend corrective actions for site-level issues.
- Support technical solution specialists in tool automation and Excel-based formulations.
- Adhere to customer-specific requirements outlined in the Statement of Work (SOW).
Qualifications and Skills
- Education: Graduate or Post-Graduate in Life Sciences or a related field.
- Experience: 2-5 years of work experience, with at least 1 year in a relevant role.
- Regulatory Knowledge: Familiarity with ICH-GCP guidelines and local regulatory requirements.
- Technical Skills: Proficiency in clinical systems like EDC, IXRS, and CTMS.
- Soft Skills: Strong communication, problem-solving, and time-management skills.
- Software Proficiency: Advanced knowledge of Microsoft Office (Word, Excel, PowerPoint).
- Attention to Detail: Ability to maintain accuracy and quality in all tasks.
Why Join IQVIA?
IQVIA is a trusted name in the pharmaceutical and healthcare industry, offering a dynamic work environment and opportunities for professional growth. By joining IQVIA as a Centralized Site Associate, you will:
- Gain exposure to global clinical trials and cutting-edge research.
- Work with a diverse and talented team of professionals.
- Enhance your skills in clinical data management and regulatory compliance.
- Contribute to improving patient outcomes through innovative healthcare solutions.
