Sumitomo Pharma
Director, Regulatory Affairs
Sumitomo Pharma, Indianapolis, Indiana, us, 46262
Sumitomo Pharma Director, Regulatory Affairs Indianapolis , Indiana Apply Now
Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. Job Overview We are currently seeking a dynamic, highly motivated, and experienced individual for the position of
Director Regulatory Affairs . The Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/she will primarily function as the Regional Regulatory Leader (RRL) and/or Global Regulatory Leader (GRL) for assigned projects. This position is expected to lead the development and implementation of regulatory strategy from proof of concept, development, registration, and post-approval for projects within the portfolio of the company. Job Duties and Responsibilities Manage and develop talent; may train/mentor junior staff. As a Regional Regulatory Lead, manage regional (United States and/or European) regulatory activities as part of a Global Regulatory Team (GRT). Leads regulatory activities for assigned project(s) in line with the global registration strategy of the product. Competently represents GRA on project team meetings. Plans, coordinates, authors, and prepares regulatory submissions and works closely with Regulatory Operations in the electronic submission. Assesses and communicates regulatory requirements ensuring activities are in compliance with applicable regulations and guidelines. Leads documentation of regulatory authority interactions including decisions and outcomes. Provides updates at the Global Regulatory Team meetings and project teams as needed. Collaborates effectively with regulatory operations leader (ROL). Maintains professional working relationship with colleagues, fostering collaboration, and idea sharing. Reviews nonclinical, clinical and CMC documentation and contributes to content as needed. Advises team members of major regulatory issues and provides possible solutions and leads the mitigation strategy. Ensures the quality and content of all submissions to Health Authorities. Leads the regional health authority meetings, liaison with local Health Authority. Document owner of briefing book documentation to Health Authorities. Assist with development of the global regulatory functional plan through research, review and interpretation of related product approvals, current regulatory guidance documents and recent public Advisory Committee proceedings. Accountable in conjunction with the GRL for developing and maintaining the development core data sheet (DCDS) if required. Ensure compliance with global regulatory requirements and adherence to regulatory internal policies and processes. Provide strategic review of dossier summaries, expert statements, and development management plans. Leads Global Regulatory Team (GRT), oversees planning and execution of global regulatory activities and submissions. Education and Experience 8 – 12 years with Master’s of relevant experience in biotech or pharmaceutical industry with minimum of 8 years focused in regulatory affairs. Master’s degree required (preferably in a scientific discipline). Compensation and Benefits The base salary range for this role is $183,000 to $228,800. Base salary is part of our total rewards package which also includes merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Sumitomo Pharma America (SMPA) is an Equal Employment Opportunity (EEO) and Affirmative Action employer . Sumitomo Pharma America (SMPA) is committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability, veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information or any other characteristic protected by law.
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Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. Job Overview We are currently seeking a dynamic, highly motivated, and experienced individual for the position of
Director Regulatory Affairs . The Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/she will primarily function as the Regional Regulatory Leader (RRL) and/or Global Regulatory Leader (GRL) for assigned projects. This position is expected to lead the development and implementation of regulatory strategy from proof of concept, development, registration, and post-approval for projects within the portfolio of the company. Job Duties and Responsibilities Manage and develop talent; may train/mentor junior staff. As a Regional Regulatory Lead, manage regional (United States and/or European) regulatory activities as part of a Global Regulatory Team (GRT). Leads regulatory activities for assigned project(s) in line with the global registration strategy of the product. Competently represents GRA on project team meetings. Plans, coordinates, authors, and prepares regulatory submissions and works closely with Regulatory Operations in the electronic submission. Assesses and communicates regulatory requirements ensuring activities are in compliance with applicable regulations and guidelines. Leads documentation of regulatory authority interactions including decisions and outcomes. Provides updates at the Global Regulatory Team meetings and project teams as needed. Collaborates effectively with regulatory operations leader (ROL). Maintains professional working relationship with colleagues, fostering collaboration, and idea sharing. Reviews nonclinical, clinical and CMC documentation and contributes to content as needed. Advises team members of major regulatory issues and provides possible solutions and leads the mitigation strategy. Ensures the quality and content of all submissions to Health Authorities. Leads the regional health authority meetings, liaison with local Health Authority. Document owner of briefing book documentation to Health Authorities. Assist with development of the global regulatory functional plan through research, review and interpretation of related product approvals, current regulatory guidance documents and recent public Advisory Committee proceedings. Accountable in conjunction with the GRL for developing and maintaining the development core data sheet (DCDS) if required. Ensure compliance with global regulatory requirements and adherence to regulatory internal policies and processes. Provide strategic review of dossier summaries, expert statements, and development management plans. Leads Global Regulatory Team (GRT), oversees planning and execution of global regulatory activities and submissions. Education and Experience 8 – 12 years with Master’s of relevant experience in biotech or pharmaceutical industry with minimum of 8 years focused in regulatory affairs. Master’s degree required (preferably in a scientific discipline). Compensation and Benefits The base salary range for this role is $183,000 to $228,800. Base salary is part of our total rewards package which also includes merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Sumitomo Pharma America (SMPA) is an Equal Employment Opportunity (EEO) and Affirmative Action employer . Sumitomo Pharma America (SMPA) is committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability, veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information or any other characteristic protected by law.
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