Pharmacovigilance Scientist - Chennai, India - Fusion Market Research

Fusion Market Research
Fusion Market Research
Verified Company
Chennai, India

2 weeks ago

Deepika Kaur

Posted by:

Deepika Kaur

beBee Recuiter
Description
Division Research and Development / Global Drug Development / Worldwide Patient Safety/Medical Safety Assessment (MSA)


Functional Area Description The Worldwide Patient Safety group is responsible for ensuring the safety of our medicines: The Worldwide Patient Safety group is responsible for pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety monitoring, safety reporting, contribution to benefit-risk assessment, risk management planning and strategy, and execution of certain post-marketing commitments and ensuring compliance with global regulatory requirements.

Position Summary Support Medical Safety Assessment Physicians (MSAP) in leading Safety Data Review (SDR) Teams.

Appropriately perform core signal detection activities and elevate program or portfolio issues impacting key Safety Managment Team (SMT) programs, priorities, resources, and milestones with appropriate oversight.

Author responses for safety data queries and contribute to specified PV sections of the Periodic Benefit Risk Evaluation Report (PBRER) and Development Safety Update Report (DSUR).

Ensure pharmacovigilance regulatory compliance with oversight, as needed. Position Responsibilities General Product Support

  • Supports Medical Safety Assessment Physician (MSAP) leading signal detection activities for a product's emerging safety profile.
  • Prepare/write PV sections of aggregate safety documents (eg, DSUR, PBRER) and analyze data for the RSI section of the IB. Write and analyze data for ad hoc responses to health authorities, with oversight.
  • Execute strategy for signal evaluation (eg, caseseries, literature review, HA/ claims database). Document signal by Safety Topic Review/ Signal Report.
  • Analyze data and prepare documentation to support label updates for assigned products, with oversight.
  • Support Safety input for regulatory product labeling.
  • Support the EU QPPV or other regional or local Qualified Person for safety issues relating to assigned products.
  • Working knowledge of product goals, strategy, drug development stage milestones, partnership agreement, HA commitments, and individual functional area responsibilities. Share with individuals and teams on these applied learnings.

Salary:
₹28, ₹30,000.45 per month


Benefits:


  • Flexible schedule

Schedule:

  • Day shift

Supplemental pay types:

  • Performance bonus

Ability to commute/relocate:

  • Chennai,

Tamil Nadu:
Reliably commute or planning to relocate before starting work (required)


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