Pharmacovigilance Vacancies in Noida: Clinical Safety/Clinical Trial ICSR Data Entry

Pharmalex Recruitment Notification

Pharmacovigilance Vacancies in Noida: Clinical Safety/Clinical Trial ICSR Data Entry including SAEs/SUSARs

About Cencora PharmaLex India

Cencora PharmaLex India is a prominent name in the pharmaceutical industry, dedicated to ensuring drug safety and regulatory compliance. With a focus on excellence and innovation, we offer a dynamic work environment that fosters growth and development.

Cencora PharmaLex India Vacancies List

  • Position Title: Pharmacovigilance Associate
  • Company Name: Cencora PharmaLex India
  • Salary: Competitive
  • Company Address: Noida, Uttar Pradesh
  • Industry Type: Pharmaceutical
  • Department: Pharmacovigilance
  • Employment Type: Full Time
  • Role Category: Clinical Safety
  • Educational Background Required: Bachelor’s/Master’s degree in Pharmacy/Life Sciences
  • Key Skills: Clinical Safety, Case Processing, SAEs/SUSARs, EDC/Clinical Databases

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Job Description

As a Pharmacovigilance Associate at Cencora PharmaLex India, you will be responsible for clinical safety and clinical trial ICSR data entry, including SAEs/SUSARs. Key responsibilities include:

About the Department & Responsibilities

The Pharmacovigilance department plays a crucial role in ensuring the safety of pharmaceutical products throughout their lifecycle. As a Pharmacovigilance Associate, you will be involved in end-to-end case processing, narrative writing, and submission of safety reports to regulatory authorities. You will collaborate with cross-functional teams to ensure compliance with regulatory requirements and facilitate timely reporting of adverse events.

Pharmalex Recruitment Notification
Pharmalex Recruitment Notification

Qualifications and Requirements

To qualify for the Pharmacovigilance Associate position, candidates must possess:

  • Educational Background: Bachelor’s/Master’s degree in Pharmacy/Life Sciences
  • Minimum Mandatory Experience: 1-3 years in clinical safety or pharmacovigilance
  • Proficiency in clinical trial ICSR data entry, including SAEs/SUSARs
  • Experience in narrative writing and case processing
  • Strong communication and organizational skills
  • Ability to work effectively in a fast-paced environment and prioritize tasks

How to Apply

If you meet the qualifications and are ready to take on this exciting opportunity, please email your application to aashi.jain@pharmalex.com. Be sure to include your resume and a cover letter highlighting your relevant experience and why you are interested in joining our team.

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