Pharmacovigilance Specialist

2 weeks ago

Chennai, Tamil Nadu, India Lifelancer Full time
Pharmacovigilance Associate Job Description

We are seeking a skilled Pharmacovigilance Associate to join our team at Lifelancer. The successful candidate will be responsible for reviewing and processing safety events, generating data listings, and maintaining project files.

Key Responsibilities:
  • Review and process safety events, including premarketing and postmarketing medical device and drug events.
  • Perform review of abstracts and full articles to identify safety information from literature sources.
  • Generate data listings from the safety database and ensure accuracy of the data.
  • Complete adverse event follow-up in writing and/or by phone based on requirements.
  • Provide input and review relevant safety tracking systems for accuracy and quality.
  • Support creation of postmarketing safety activities, such as PSMF, RMP, and PBRER.
  • Liaise with investigational site reporters and/or sponsors as necessary regarding safety issues.
  • Attend project team and sponsor meetings and teleconferences as required.
Requirements:
  • Experience in a Pharmaceutical/CRO environment.
  • At least 1 year of experience in the pharmacovigilance area.
  • Excellent verbal and written communication skills.
  • Detail-oriented.
  • Fluent in written and verbal English.
  • Excellent organizational and time management skills.

Lifelancer is a talent-hiring platform in Life Sciences, Pharma, and IT. We connect talent with opportunities in pharma, biotech, health sciences, healthtech, data science, and IT domains. If you are interested in this role, please use the below Lifelancer link for job application and quicker response.

/jobs/view/695006a94213e58da56a487259b13915

Remote work: No

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