PE-Pharmacovigilance

5 days ago

Taguig, National Capital Region, Philippines Cognizant Technology Solutions Full time ₱900,000 - ₱1,200,000 per year

Job Summary

Join our dynamic team as a Pharmacovigilance Associate where you will play a crucial role in ensuring the safety and efficacy of pharmaceutical products. With a focus on Pharma Research & Development you will contribute to the monitoring and evaluation of drug safety data. This hybrid role offers the flexibility of rotational shifts providing a comprehensive experience in the field.

Responsibilities

  • Monitor and evaluate adverse event data to ensure drug safety and compliance with regulatory standards.
  • Collaborate with cross-functional teams to support the development and implementation of safety monitoring plans.
  • Assist in the preparation and submission of safety reports to regulatory authorities.
  • Conduct thorough research and analysis of safety data to identify potential risks and trends.
  • Support the development of risk management strategies to mitigate identified risks.
  • Participate in the review and assessment of safety information from clinical trials and post-marketing sources.
  • Provide input and support for the development of safety-related documents and reports.
  • Maintain accurate and up-to-date records of safety data and case processing activities.
  • Ensure compliance with standard operating procedures and regulatory requirements.
  • Contribute to the continuous improvement of pharmacovigilance processes and systems.
  • Collaborate with team members to ensure timely and accurate case processing.
  • Engage in ongoing training and development to stay current with industry best practices.
  • Support the implementation of new pharmacovigilance tools and technologies. Qualifications
  • Possess a degree in a relevant scientific field such as pharmacy or life sciences.
  • Demonstrate strong analytical and problem-solving skills with attention to detail.
  • Exhibit excellent communication and interpersonal skills for effective collaboration.
  • Show proficiency in using pharmacovigilance databases and software.
  • Have a basic understanding of regulatory requirements and guidelines.
  • Display a keen interest in drug safety and pharmacovigilance practices.
  • Experience in PV Case Processing is a plus.

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