Drug Safety Associate

Roles & Responsibilities
• Collect, review, and process Adverse Event (AE) and Serious Adverse Event (SAE) reports
• Perform case processing and data entry in drug safety databases
• Ensure accuracy, completeness, and timeliness of safety case documentation
• Conduct literature search and review for safety-relevant information
• Assist in signal detection, risk assessment, and safety evaluations
• Support preparation and submission of safety reports such as PSURs and DSURs
• Ensure compliance with ICH-GCP, ICH-E2B, and global regulatory guidelines
• Coordinate with cross-functional teams including Clinical, Regulatory, and Quality
• Maintain safety records and support audit and inspection readiness

Qualification
• Bachelor’s degree in Pharmacy, Life Sciences, Nursing, or a related discipline

Experience
• 0 to 2 years of experience in Pharmacovigilance or Drug Safety
• Freshers with relevant academic knowledge may also apply

Skills
• Basic knowledge of pharmacovigilance and drug safety concepts
• Understanding of AE/SAE reporting and regulatory requirements
• Good written and verbal communication skills
• Strong attention to detail and analytical skills
• Ability to work independently and in a team environment
• Proficiency in MS Word, Excel, and safety databases is an advantage

About the Organization
Jeevan Scientific Technology Limited is a leading life sciences and healthcare solutions company offering services across pharmacovigilance, clinical research, regulatory affairs, and data management. The organization supports global pharmaceutical and biotech companies with high-quality, compliant, and technology-driven solutions.