Dr. Reddy’s Laboratories Recruitment Pharmacovigilance Systems and Safety Data Lead

Dr. Reddy’s Laboratories Recruitment July 2020 B. Pharm, M. Pharm, Life Science Post Graduate. for Pharmacovigilance Systems and Safety.

Vacancy details:

  • Post Name: Pharmacovigilance Systems and Safety Data Lead
  • Education : B. Pharm, M. Pharm, Life Science Post Graduate.
  • Experience: Ideally 6+ years experience in the Pharma industry in either a pharmacovigilance data entry or Pharma IT role, but 2+ years must be in safety database management
  • Location: Hyderabad
  • Address :8-2-337, Road No 3,, Hyderabad, Telangana, India
  • Salary :  INR 20,00,000 – 30,00,000 PA.
  • Openings : NA
  • Contact Person: HR

 Job Description: We have requirement for the post of Pharmacovigilance Systems and Safety Data Lead in Dr. Reddy’s Laboratories.

Responsibilities:

  • Act as the PV Subject Matter Expert for the global safety database and associated systems
  • Act as the primary liaison and first point of contact for:
    • Internal DRL IT in support of safety database maintenance and changes
    • The vendor supplier of the safety database and associated systems
  • Provide system administration support for central safety database applications as appropriate
  • Coordinate, implement and provide training for PV system projects and follow through the full project life-cycle
  • Develop user requirements, functional specifications and propose solutions for unmet safety system business needs
  • Analyze, collect, test, implement, and maintain safety database configuration changes
  • Perform quality control check on configuration changes; identify discrepancies between the request and the implementation and resolve them or initiate their resolution
  • Support testing and validation processes for pharmacovigilance IT projects; including generation of the appropriate documentation
  • Develop, provide support to create complex specialized data outputs from the safety database for various Pharmacovigilance reports/ad hoc queries, as appropriate
  • Ensure understanding of pharmacovigilance requirements and processes to support process improvement initiatives and the implementation of regulatory changes
  • Provide training to new team members on the PV system, as required
  • Provide safety database SME support during audit and Regulatory Authority Inspections

Selection Process: The selection will be on the basis of Interview.

How to Apply Click here for full details and Apply Online

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