Luminary Group is hiring a
Oncology Physician

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Luminary Group

πŸ’΅ ~$112k-$161k
πŸ“Remote - People's Republic of China

Summary

The job is for a Safety Physician specializing in Oncology who will ensure the safety and efficacy of oncology products for a pharmaceutical consulting company's operations in China. The role involves overseeing safety management, conducting safety surveillance, contributing to risk management plans, providing medical input during safety reviews, collaborating with cross-functional teams, monitoring and communicating emerging safety concerns, participating in regulatory interactions, staying updated with oncology drug safety regulations, and ensuring effective communication of safety information.

Requirements

  • Medical degree (MD) with specialization in oncology or related field
  • Minimum of 3 years of experience in pharmacovigilance or drug safety, preferably in the oncology therapeutic area
  • Strong knowledge of pharmacovigilance practices and regulations in China
  • Understanding of oncology drug development and regulatory requirements
  • Experience in safety evaluation of adverse events and signal detection
  • Familiarity with risk management plans and safety aggregate reports
  • Effective communication and collaboration skills to work with cross-functional teams
  • Ability to analyze and interpret complex safety data
  • Proficiency in both written and spoken Chinese and English languages
  • Able to work independently and prioritize tasks effectively
  • Authorization to work in China

Responsibilities

  • Oversee the safety management of oncology products throughout their lifecycle
  • Conduct safety surveillance and evaluation of adverse events and other safety data
  • Contribute to the development and implementation of risk management plans
  • Provide medical input and expertise during safety reviews and signal detection activities
  • Collaborate with cross-functional teams to review and interpret safety data for regulatory submissions
  • Conduct medical assessment of individual case safety reports and contribute to safety aggregate reports
  • Monitor and communicate emerging safety concerns and trends to internal and external stakeholders
  • Participate in safety-related regulatory interactions and support regulatory inspections and audits
  • Stay updated with the latest developments and regulations related to oncology drug safety
  • Collaborate with medical affairs and other teams to ensure safety information is effectively communicated to healthcare professionals and patients

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