Remote Oncology Physician

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