Manager, Regulatory Affairs

Job DescriptionWe are seeking an experienced regulatory professional to support global regulatory activities across early- and late-stage development programs through lifecycle management. The Manager, Regulatory Affairs will partner cross-functionally to support high-quality regulatory submissions and help drive successful interactions with global health authorities.This role will support regulatory strategy and execution for submissions including INDs, CTAs, NDA components, supplements, and other product-related regulatory activities. The ideal candidate brings strong knowledge of U.S. and international regulatory requirements, excellent collaboration skills, and the ability to manage multiple priorities in a fast-paced environment.Key ResponsibilitiesSupport preparation, review, and submission of regulatory filings including INDs/CTAs, amendments and information requisitions, Orphan drug applications, Annual Reports, and Investigator’s Brochures.Assist in coordination and preparation of global health authority meeting documents.Contribute to global regulatory strategy and ensure submissions meet health authority requirements and quality standards.Represents regulatory for global study-level regulatory activities included but not limited to study start-up, study maintenance, and end of trial activities.Collaborate with external partners and vendors on regulatory activities and submission support.Support regulatory operations and continuous improvement initiatives, including work instruction and SOP development and maintenance.QualificationsQualificationsBachelor’s degree, preferably in a scientific discipline.6+ years of pharmaceutical industry experience, including 4+ years in Regulatory Affairs.Strong knowledge of U.S. and international regulatory requirements for drug development.Excellent verbal and written communication, organizational, and cross-functional collaboration skills.Strong experience in a self-motivated, fast-paced environmentExperience supporting initial INDs/CTAs, and initial marketing application activities is highly desirable.Additional InformationDeciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $116,000 - $160,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.​Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Deciphera’s competitive total rewards strategy that also includes annual performance bonus, a long-term incentive plan, full range of benefits and other incentive compensation plans (if applicable)Benefits:Competitive salary and annual bonus.Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more.Generous parental leave and family planning benefits.Outstanding culture and opportunities for personal and professional growth.EQUAL EMPLOYMENT OPPORTUNITY INFORMATIONDeciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis.SummaryType: Full-timeFunction: ScienceExperience level: AssociateIndustry: Pharmaceuticals