Data Solutions Coordinator

2 days ago

Rajahmundry, Andhra Pradesh, India beBeeRegulatoryAffairs Full time ₹ 50,00,000 - ₹ 1,00,00,000

We are seeking a skilled professional to play a critical role in monitoring and analyzing the global regulatory landscape within the life sciences industry.

The ideal candidate will be responsible for supporting our products and services by participating in global monitoring, surveillance, and data acquisition activities. The primary focus will be on ensuring the accuracy and integrity of our regulatory data while working closely with cross-functional teams to identify emerging trends in the pharmaceutical and MedTech regulatory environments.

Key Responsibilities:
  • Monitor and track global regulatory information related to the life sciences industry.
  • Maintain awareness of current and relevant regulations, guidelines, policies, procedures, and practices.
  • Analyze and evaluate regulatory data, rules, and guidance document changes to make informed decisions.
  • Collaborate with teams to identify and assess emerging trends in the pharmaceutical and medtech regulatory environments.
  • Conduct data quality checks to ensure accuracy, completeness, and integrity of regulatory data.
Requirements:
  • 2-4 years of experience in pharmaceutical or medical device industries, focusing on regulatory affairs or quality assurance.
  • A Master's degree (M.S.) in Regulatory Affairs or Quality Assurance is preferred.
Essential Skills:
  • Effective communication skills to share regulatory intelligence insights, updates, and trends with teams and stakeholders.
  • Ability to analyze and evaluate regulatory data to make informed decisions.
  • Organizational skills to prioritize multiple time-sensitive projects related to monitoring and tracking global regulatory information.
  • Commitment to continuous learning to stay updated on the evolving global regulatory landscape.
  • Tech savvy skills to leverage digital tools and technology solutions to monitor regulatory changes.

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