Pharmacovigilance Specialist Hiring at ProPharm

Pharmacovigilance Specialist Hiring at ProPharma

ProPharma, the world’s largest Research Consulting Organization (RCO), is hiring a Pharmacovigilance Specialist in India. If you have a passion for ensuring the safety of medicines and a background in life sciences, this is a fantastic opportunity to grow your career at a leading global firm. ProPharma has been improving patient health and wellness for over 20 years, and now, they’re looking for a dedicated individual to join their Pharmacovigilance team.

About ProPharma Group

ProPharma is a top-tier Research Consulting Organization (RCO) providing expertise to biotech, medical device, and pharmaceutical companies. With deep expertise in regulatory sciences, clinical research solutions, quality and compliance, pharmacovigilance, medical information, and R&D technology, ProPharma supports organizations through the entire product lifecycle. As an advisor and partner, they help companies introduce innovative therapies safely and efficiently.

Current Vacancies: Pharmacovigilance Specialist Role

ProPharma is actively hiring a Pharmacovigilance Specialist to join its dynamic team in India. This position is critical for processing adverse event cases, ensuring that patients receive the highest standard of care and safety monitoring.

Required Qualifications

• Essential Education: A Bachelor’s degree in Life Sciences (e.g., BSc, BTech, MSc in Biology, Microbiology, Biotechnology).
• Preferred Education: Advanced degrees such as RN, RPh, PharmD, or equivalent.
• Experience Required: At least two years of relevant work experience in Pharmacovigilance or related fields.

Key Responsibilities of the Pharmacovigilance Specialist

As a Pharmacovigilance Specialist at ProPharma, you will be responsible for various critical tasks to support patient safety and regulatory compliance:

• Responsible for daily case processing of adverse event cases (clinical trial and/or post marketed), including coding using MedDRA, determining seriousness and expectedness at the event and case level.
• Perform case follow up activities such as identification of information to be collected during follow-up.
• Creating and reviewing case narratives.
• Providing client notifications as required for case management.
• Supporting and contributing to the development of training materials and training delivery.
• Highlight areas of concern/discrepancies to the Principal PV Specialist, Case Processing and/or Manager, Case Processing when related to ICSRs.
• Acquire and maintain an up-to-date knowledge of global safety regulations for medicines.
• Peer reviews of cases for quality, consistency, and accuracy as needed.
• Other duties as assigned

Skills and Abilities Needed

ProPharma is looking for a candidate with the following skills and abilities:

• Strong verbal and written communication skills to ensure clear and concise reporting.
• A high level of attention to detail and accuracy to handle sensitive patient safety data.
• Problem-solving capabilities to identify and resolve discrepancies in case processing.
• Ability to work independently and as part of a collaborative, multi-disciplinary team.
• Excellent organizational skills and the ability to prioritize tasks effectively.

How to Apply

If you’re a skilled Pharmacovigilance professional with a passion for ensuring patient safety, apply today for this exciting opportunity at ProPharma. Submit your resume through the official application portal:

Apply for Pharmacovigilance Specialist Role at ProPharma

Tagged as: Global Pharma Jobs, Good Clinical Practice (GCP), Pharmaceutical Careers