Posted:1 day ago| Platform: Shine logo

Apply

Work Mode

On-site

Job Type

Full Time

Job Description

 

  • Reviewing and evaluating adverse event reports to determine if they meet regulatory reporting requirements.
  • Entering and maintaining adverse event information in safety databases
  • Narrative writing
  • Communicating with healthcare professionals and other stakeholders to gather additional information about adverse events
  • Assisting in the preparation of safety reports to be submitted to regulatory agencies
  • Monitoring safety literature to stay current on the latest safety information related to the products
  • Collaborating with other departments such as clinical research, regulatory affairs, and pharma covigilance to ensure compliance with safety regulations and guidelines
  • Participating in the development and implementation of safety policies and procedures
  • Reviewing and assessing the safety profile of new and existing products
  • Participating in the development and execution of risk management plans
  • Communicating with regulatory authorities, healthcare professionals, and other stakeholders on safety-related issues.

Mock Interview

Practice Video Interview with JobPe AI

Start Job-Specific Interview
cta

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.

Job Application AI Bot

Job Application AI Bot

Apply to 20+ Portals in one click

Download Now

Download the Mobile App

Instantly access job listings, apply easily, and track applications.

coding practice

Enhance Your Skills

Practice coding challenges to boost your skills

Start Practicing Now

RecommendedJobs for You

mumbai city, bilaspur, anantnag, gwalior, cuttack, kannur, wayanad, ambala, patna, coimbatore

Bengaluru, Karnataka, India

Hyderabad, Bengaluru, Mumbai (All Areas)