What are the responsibilities and job description for the Senior Pharmaceutical Manager position at Takeda?
About the Role
Join our team as a Senior Manager, US Medical Ad/Promo Regulatory Review where you will contribute to the development of innovative pharmaceuticals and patient support programs.
As a member of our team, you will be responsible for providing regulatory strategic oversight for at least one complex product or therapeutic area/multiple products. This includes ensuring regulatory compliance of promotional materials generated for assigned US products and compounds. You will work closely with cross-functional teams to achieve this goal.
Responsibilities include understanding and interpreting complex issues related to regulatory requirements and promotional strategy, mentoring and developing staff, and chairing promotional review meetings. You will also present regulatory topics to senior management and cross-functional teams.
In addition to these responsibilities, you will maintain current knowledge of applicable government regulations, particularly those related to advertising and promotion. You will also provide regulatory guidance to drug development teams and contribute to clinical study design discussions.
Our comprehensive benefits package includes medical, dental, vision insurance, 401(k) plan, short-term and long-term disability coverage, basic life insurance, tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits.
Join our team as a Senior Manager, US Medical Ad/Promo Regulatory Review where you will contribute to the development of innovative pharmaceuticals and patient support programs.
As a member of our team, you will be responsible for providing regulatory strategic oversight for at least one complex product or therapeutic area/multiple products. This includes ensuring regulatory compliance of promotional materials generated for assigned US products and compounds. You will work closely with cross-functional teams to achieve this goal.
Responsibilities include understanding and interpreting complex issues related to regulatory requirements and promotional strategy, mentoring and developing staff, and chairing promotional review meetings. You will also present regulatory topics to senior management and cross-functional teams.
In addition to these responsibilities, you will maintain current knowledge of applicable government regulations, particularly those related to advertising and promotion. You will also provide regulatory guidance to drug development teams and contribute to clinical study design discussions.
Our comprehensive benefits package includes medical, dental, vision insurance, 401(k) plan, short-term and long-term disability coverage, basic life insurance, tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits.
