Director Regulatory Oncology
Company Name:
Koch Davis
Accountable for leading or contributing to the preparation of global regulatory strategy and implementation plan, core label, risk register for assigned project. Develop and maintain constructive working relationship with health authority contact. Ensure an aligned regulatory position is reached and communicate for all key issues for assigned project, and that these regulatory position supporting the business are championed and communicated. Work closely with other regulatory strategist within and across site to ensure consistent and appropriate process, system, working practice, shared learning and quality standard. Ensure business compliance, and implementation of and adherence to regulatory standard.
Job Requirements
Prior oncology drug development experience preferred. Proven ability to manage complex regulatory issue. Proven ability to consistently deliver within time, cost and quality standard. Ability to communicate complex information and analyses to a variety of audiences in both verbal and written format, and to effectively work with global, cross functional team.
Education
Bachelor degree
Client
The client is a multinational pharmaceutical corporation which develops and produces medicines and vaccines for a wide range of medical disciplines.Estimated Salary: $20 to $28 per hour based on qualifications.
Koch Davis
Accountable for leading or contributing to the preparation of global regulatory strategy and implementation plan, core label, risk register for assigned project. Develop and maintain constructive working relationship with health authority contact. Ensure an aligned regulatory position is reached and communicate for all key issues for assigned project, and that these regulatory position supporting the business are championed and communicated. Work closely with other regulatory strategist within and across site to ensure consistent and appropriate process, system, working practice, shared learning and quality standard. Ensure business compliance, and implementation of and adherence to regulatory standard.
Job Requirements
Prior oncology drug development experience preferred. Proven ability to manage complex regulatory issue. Proven ability to consistently deliver within time, cost and quality standard. Ability to communicate complex information and analyses to a variety of audiences in both verbal and written format, and to effectively work with global, cross functional team.
Education
Bachelor degree
Client
The client is a multinational pharmaceutical corporation which develops and produces medicines and vaccines for a wide range of medical disciplines.Estimated Salary: $20 to $28 per hour based on qualifications.
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