Senior Clinical Study Specialist

2 days ago

Mumbai, Maharashtra, India beBeeClinicalResearch Full time ₹ 6,00,000 - ₹ 9,00,000 per year

Job Overview

  • Conduct site assessments to determine feasibility of clinical studies

Key Responsibilities:

  • Negotiate with investigators to finalize study budgets and timelines
  • Coordinate the preparation and submission of study documents for ethics committee approval
  • Oversee inventory management, IP dispensing, and reconciliation processes
  • Ensure timely initiation, monitoring, and close-out activities at clinical sites
  • Provide training to investigators and site personnel on study protocols, procedures, and GCP principles

Requirements:

  • Hold a Bachelor's or Master's degree in a health-related field
  • Possess 1-5 years of relevant experience in clinical research

Why This Role Matters

This is an exciting opportunity to contribute to the advancement of medical knowledge and improve patient outcomes.

We are seeking a highly motivated and experienced Clinical Research Associate to join our team.

The ideal candidate will possess excellent communication and project management skills, as well as a strong understanding of clinical research principles and regulations.

As a Clinical Research Associate, you will play a critical role in ensuring the successful execution of clinical studies from start to finish.

Key Performance Indicators (KPIs)

  • Site assessment completion rates
  • Study document submission and ethics committee approval rates
  • Inventory management and IP dispensing accuracy rates
  • Timely site initiation, monitoring, and close-out activities
  • Investigator and site personnel training satisfaction ratings

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