Are you passionate about patient safety and looking for a rewarding career in pharmacovigilance? Novaspire Biosciences is hiring for a Pharmacovigilance Technical Role in Bengaluru, Karnataka, India, and this could be your chance to shine in 2025! This full-time, on-site position offers an exciting opportunity to work with a leading healthcare company dedicated to advancing pharmacovigilance, clinical research, and public health. Read on to discover why this job at Novaspire Biosciences could be your next big career move, how to tailor your resume, and tips to position yourself as the perfect candidate.
Why Join Novaspire Biosciences in Bengaluru?
Novaspire Biosciences Private Limited is a trusted name in the healthcare industry, specializing in Pharmacovigilance, Clinical Research, and Bioavailability/Bioequivalence studies. Based in Bengaluru—India’s thriving biotech hub—this company is committed to ensuring patient safety through innovative solutions for the pharmaceutical and biotechnology sectors. With a team of seasoned professionals excelling in regulatory compliance, data management, and medical writing, Novaspire Biosciences offers a dynamic work environment where your skills can make a real impact.
For this Pharmacovigilance Technical Role, you’ll be part of a mission-driven organization that values expertise and dedication. Whether you’re a B.Pharm or M.Pharm graduate with clinical experience, this job in Bengaluru could elevate your career in 2025.
What Does the Pharmacovigilance Technical Role Entail?
This full-time, on-site position at Novaspire Biosciences in Bengaluru involves critical responsibilities in pharmacovigilance processes. Here’s how you’ll spend your day in this exciting role:
- Adverse Event Reporting: Collect, review, and process adverse event reports (AERs) from healthcare professionals, patients, and clinical trials, ensuring accurate data entry into safety databases.
- MedDRA Coding: Assign precise Medical Dictionary for Regulatory Activities (MedDRA) codes to classify adverse events effectively.
- Signal Detection: Analyze adverse event data to spot potential safety signals that need further investigation.
- Risk Assessment: Evaluate the severity and frequency of adverse events to assess medication risk-benefit profiles.
- Regulatory Reporting: Submit timely reports of serious adverse events (SAEs) and suspected unexpected serious adverse reactions (SUSARs) to regulatory authorities.
- Compliance: Uphold Good Pharmacovigilance Practices (GVP) and adhere to local regulatory standards.
This Pharmacovigilance Technical Role is perfect for detail-oriented professionals who thrive in ensuring drug safety and regulatory excellence.
Are You a Good Fit for This Job at Novaspire Biosciences?
To succeed in this role at Novaspire Biosciences, you’ll need the right qualifications and experience. Here’s what the company is looking for:
- Qualifications: B.Pharm or M.Pharm degree.
- Experience: 3-5 years of clinical medical experience, plus 1-2 years in pharmacovigilance (PV). Bonus points if you have Clinical Operations (ClinOps) experience!
- Skills: Expertise in adverse event reporting, MedDRA coding, signal detection, risk assessment, and regulatory compliance.
