Site Report Review Specialist

6 days ago

Bengaluru, Karnataka, India beBeeClinicalResearchAssociate Full time ₹ 6,00,000 - ₹ 8,00,000
Project Overview
Clinical Research Associates (CRAs) play a vital role in ensuring the integrity and quality of clinical trials. As an Associate Site Report Specialist, you will be responsible for reviewing site visit reports to ensure they meet or exceed quality standards.

Key Responsibilities
  • Review site visit reports (SVRs) to ensure they meet quality standards and support project goals.
  • Provide guidance to Clinical Project Managers on SVR annotations and training.
  • Identify and track project team compliance with SOPs for submission and approval of SVRs.
  • Participate in project team review activities and escalate issues, trends, and risk factors to optimize quality delivery.

Requirements
  • 4-6 years of relevant experience as a Clinical Research Associate.
  • Minimum of 3-4 years of on-site monitoring experience.

Benefits

This is a home-based opportunity that offers flexibility and work-life balance. As a valued member of our team, you will have the opportunity to grow and develop your skills in a supportive and collaborative environment.


What We Offer

We offer competitive compensation packages, comprehensive benefits, and opportunities for professional growth and development.

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