Pharmacovigilance Technical Hiring Novaspire Biosciences
Job Overview
Company: Novaspire Biosciences
Position: Pharmacovigilance Technical Role
Experience: 3-5 Years
Location: Bengaluru, India
Education: B.Pharm, M.Pharm
Application Deadline: February 20, 2025
Why Join Novaspire Biosciences?
✅ Leading Healthcare Company: Specializing in Pharmacovigilance, Clinical Research, and Bioavailability/Bioequivalence studies.
✅ Work-Life Balance: Flexible work policies for professional growth and well-being.
✅ Challenging Projects: Engage in cutting-edge pharmacovigilance initiatives.
✅ Competitive Salary & Benefits: Health insurance, retirement plans, and career development programs.
Pharmacovigilance Technical Hiring Novaspire
Key Responsibilities
- Collect, review, and process adverse event reports (AERs) from various sources.
- Assign Medical Dictionary for Regulatory Activities (MedDRA) codes to classify adverse events.
- Analyze adverse event data to identify potential safety signals.
- Assess risk by evaluating severity and frequency of adverse events.
- Prepare and submit regulatory reports, including Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs).
- Ensure compliance with Good Pharmacovigilance Practices (GVP) and regulatory guidelines.
Required Skills & Qualifications
- Degree: B.Pharm or M.Pharm.
- Experience: 3-5 years in clinical medical settings, with at least 1-2 years in Pharmacovigilance.
- Technical Expertise: Proficiency in adverse event reporting, MedDRA coding, signal detection, and risk assessment.
- Regulatory Knowledge: Strong understanding of pharmacovigilance compliance and local/global regulations.
🚀 Be Part of a Mission-Driven Organization – Apply Now! Pharmacovigilance Technical Hiring Novaspire
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