Pharmacovigilence / Clinical Research specialist

0 - 2 years

2 Lacs

Posted:18 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Clinical trials is a crucial field in the pharmaceutical industry focused on drug safety. Professionals in this area monitor, assess, and prevent adverse drug reactions to protect public health.


Qualification & Specifications :

MBBS,BDS,BHMS,BAMS,BSMS,PHARMACYB.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDIAL, B.Tech (Biotechnology/Bio Chemistry).

2020 -2024 passed out

Skills Required:

  • Scientific Background:

    Degree in Pharmacy, Life Sciences, or Medicine.
  • Attention to Detail:

    Meticulous accuracy in data entry and documentation.
  • Analytical Skills:

    Ability to analyze data and identify safety signals.
  • Regulatory Knowledge:

    Understanding of Good Pharmacovigilance Practices (GVP) and other regulations.

Key Responsibilities:

  • Case Processing:

    Receive, document, and process reports of adverse drug reactions (ADRs) from various sources, ensuring accurate data entry into safety databases.
  • Signal Detection:

    Analyze safety data to identify new risks or trends associated with a drug.
  • Risk Management:

    Develop and implement strategies to mitigate identified risks, ensuring the drug's benefits outweigh its potential harms.
  • Regulatory Reporting:

    Prepare and submit safety reports (e.g., PSURs) to regulatory authorities, ensuring compliance with global guidelines.
  • Documentation:

    Create and maintain accurate and compliant scientific and regulatory documents, including Standard Operating Procedures (SOPs) and safety reports.

For more details contact


Kowshika (HR)

7200652461
Mail to- trichy@resolveitech.com

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Resolve Medicode

Hospitals and Health Care

Coimbatore Tamilnadu

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