Regulatory Affairs, Pharmacovigilance, Bioinformatician, Clinical Data Management,

Summary

I have 1 year of experience in the pharmaceutical regulatory industry. I have experience working with RIMS (Regulatory Information Management System) Product Life Cycle Management, Database management, Process improvement, and IDMP Data readiness-related Data Analysis. I am actively seeking learning opportunities to grow and build a successful career in Life Sciences.
I am adept at interpreting and applying regulatory guidelines and preparing necessary documentation and analysis for implementation.

Expectations

Good working environment, Opportunities to grow, On-Site opportunities, Work-life balance

Employment Preferences

Expected Base Salary

**0,000 INR

Academic Degree

Experience

Skills

• Pharmaceutical Regulatory Affairs
• Regulatory Information Management System
• LS RIMS
• IDMP
• Data Analysis
• MS Office
• Scientific Writing
• Client
• Interpersonal Communication
• Time Management
• Attention To Detail
• Analytical Mindset
• Fast Learner