Site Quality Review Specialist
4 days ago
Job Title: Site Quality Review Specialist
">We are seeking a highly skilled and detail-oriented Site Quality Review Specialist to join our team. In this role, you will be responsible for reviewing Site Visit Reports (SVRs) to ensure they meet or exceed quality standards.
">The ideal candidate will have 4-6 years of experience in clinical research, with a strong understanding of GCP guidelines, ICH regulations, and IQVIA SOPs.
">You will work closely with Clinical Project Managers to provide guidance and support, ensuring compliance with protocol requirements and timelines.
">In addition, you will identify and track project team compliance with SOPs, communicate with CRAs and line managers, and participate in project team activities.
">To succeed in this role, you must have excellent analytical skills, attention to detail, and effective communication skills.
">Required Skills:
">- ">
- Minimum 3-4 years on-site monitoring experience">
- Basic therapeutic and protocol knowledge">
- Clinical Research Associate (CRA) experience">
Techincal Skills:
">Proficient in using tools and techniques to ensure the efficient and effective review of Site Visit Reports and their associated attachments.
">Benefits:
">This is an exciting opportunity to work in a dynamic and growing organization, with opportunities for career growth and development.
">About Us:
">We are a leading provider of clinical trial solutions, dedicated to delivering high-quality services that meet the needs of our clients and patients.
"] ,-
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