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Pro Pharma Hiring Pharmacovigilance Specialist

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ProPharma Group

2 Years

Hyderabad

B.Pharm, M.Pharm, Pharm.D, Lifesciences, Advanced degree, RN, RPh, equivalent

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Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

Are you a skilled professional with a passion for pharmacovigilance and patient safety? ProPharma Group, a global leader in Research Consulting Organizations (RCOs), is hiring a Pharmacovigilance Specialist for its Hyderabad location. This is a full-time opportunity to join a team dedicated to advancing healthcare and ensuring the safety of pharmaceutical products. If you have a background in life sciences and experience in pharmacovigilance, this could be the perfect role for you.

About ProPharma Group
For over 20 years, ProPharma Group has been at the forefront of improving patient health and wellness. As the world’s largest RCO, ProPharma partners with biotech, medical device, and pharmaceutical companies to provide end-to-end consulting solutions. Their expertise spans regulatory sciences, clinical research, quality & compliance, pharmacovigilance, medical information, and R&D technology. By leveraging their advise-build-operate model, ProPharma helps clients navigate the complexities of the product lifecycle, ensuring the safe and timely introduction of new therapies.

Job Overview
As a Pharmacovigilance Specialist, you will play a critical role in ensuring the safety of pharmaceutical products by managing adverse event cases. This position requires a high level of attention to detail, strong communication skills, and a solid understanding of global pharmacovigilance regulations.

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Key Responsibilities

  • Process adverse event cases (clinical trial and post-marketed) daily, including coding using MedDRA and determining seriousness and expectedness.
  • Conduct case follow-up activities to gather additional information as needed.
  • Create and review case narratives to ensure accuracy and completeness.
  • Notify clients of critical case-related information.
  • Contribute to the development and delivery of training materials.
  • Identify and escalate discrepancies or concerns to the Principal PV Specialist or Manager.
  • Stay updated on global pharmacovigilance regulations and guidelines.
  • Perform peer reviews of cases to ensure quality, consistency, and accuracy.
  • Collaborate with cross-functional teams to achieve organizational goals.

Required Skills and Qualifications

  • Education: Bachelor’s degree in life sciences (required). Advanced degree, RN, RPh, PharmD, or equivalent (preferred).
  • Experience: Minimum of 2 years of pharmacovigilance or related work experience.
  • Strong verbal, written, and interpersonal communication skills.
  • High attention to detail and accuracy.
  • Ability to identify and resolve problems efficiently.
  • Excellent organizational and multitasking abilities.
  • Basic knowledge of pharmacovigilance principles and practices.

Why Join ProPharma Group?
ProPharma Group is committed to fostering a diverse, equitable, and inclusive workplace. They celebrate differences and encourage employees to bring their authentic selves to work. With a focus on innovation, collaboration, and entrepreneurship, ProPharma provides a supportive environment where employees can thrive.

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