{"id":4054054,"url":"https://alion.io/job/exelixis-sr-regulatory-operations-manager","title":"Sr Regulatory Operations Manager","company":{"id":1917987,"name":"Exelixis","domain":"exelixis.com","url":"https://alion.io/company/exelixis-com","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":null},"role":"Management","role_family":"Management","seniority":"senior","employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"board_field","remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Alameda, United States"],"countries":["US"],"hiring_countries":["US"],"hiring_countries_total":1,"salary":{"min":165000,"max":208500,"currency":"USD","period":"year","gross":null,"usd_annual":208500},"salary_estimate":null,"experience_years_min":9,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Veeva","optional":false}],"status":"live","first_seen_at":"2026-11-10T00:00:00Z","employer_posted_date":"2026-11-10","last_verified_at":"2026-11-11T20:33:53Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"SUMMARY/JOB PURPOSE\nManage and independently execute regulatory submission planning, publishing, quality control, delivery, archiving and lifecycle management for clinical and commercial programs. Provide eCTD technical expertise and manage submission plans in Veeva RIM to ensure timely, high-quality submissions that meet Health Authority requirements and company standards. Implement evolving FDA requirements and collaborate on process, technology and automation improvements to enhance efficiency, compliance and scalability.\nESSENTIAL DUTIES/RESPONSIBILITIES\nIndependently format, publish, transmit and archive Health Authority submission types, ensuring submissions are high quality, compliant and delivered according to established timelines.\nServe as subject matter expert for regulatory publishing and document management technologies such as LORENZ docubridge, Veeva Vault RIM, Microsoft Word, Adobe Acrobat and regulatory validation tools, as applicable.\nProvide Regulatory Operations expertise and guidance on eCTD structure, content readiness, publishing requirements, validation, dispatch and lifecycle management in accordance with Health Authority requirements.\nPerform document- and submission-level technical quality control to ensure completeness, consistency, accuracy and compliance with company standards and regulatory requirements.\nIdentify IT solutions to enhance Regulatory Operations capabilities in document formatting and submission publishing, automation opportunities and technology enhancements that improve submission quality, efficiency, compliance and scalability.\nCreate regulatory submission objectives, submission content plans, and documentation within Veeva RIM.\nRoutinely participate in the review of evolving FDA electronic submission requirements and technical standards, assess operational impact and implement changes as appropriate.\nCollaborate within Regulatory Operations on SOPs, work instructions, templates, checklists, standards and best practices that support consistent and efficient Regulatory Operations processes.\nPerforms other duties as assigned\nComplies with all policies and standards\nSUPERVISORY RESPONSIBILITIES\nNone.\nEDUCATION/EXPERIENCE/KNOWLEDGE/SKILLS & ABILITIES\nEducation\nBachelor’s degree in related discipline and a minimum of nine years of related experience; or,\nMaster’s degree in related discipline and a minimum of seven years of related experience; or,\nPhD degree in related discipline and a minimum of two years of related experience; or,\nEquivalent combination of education and experience.\nKnowledge, Skills and Abilities\nRequired:\nSubject matter expert for regulatory publishing and document management technologies such as LORENZ docubridge, Veeva Vault RIM, Microsoft Word, Adobe Acrobat and regulatory validation tools.\nManages time and resources to complete tasks and achieve results within established timelines. Takes pride in delivering high quality work.\nApplies knowledge of the regulatory framework and industry practices to complete routine work.\nDemonstrates clear and effective verbal and written communication. Provides timely and appropriate information updates. Speaks clearly and confidently in one-to-one situations and effectively presents information to small groups of departmental colleagues.\nGood interpersonal skills and emerging ability to accommodate differing views to support the development of an agreed upon resolution.\nWorks collaboratively with team members to achieve common objectives. Engages internal stakeholders to establish collaborative relationships.\nApplies knowledge of organizational objectives and demonstrates skill and insight in gathering, analyzing and applying key information to solve problems.\nLeads self by managing and executing own work. Acts with integrity and builds trust with colleagues to contribute to accomplishing team objectives.\n Travel Requirements\n20% Travel approximately 20%\nLocation: Remote\n\nRange for this position: $165,000 - $208,500\n\nThe base pay offered will take into account job-related knowledge, skills, experience and internal equity, among other factors.In addition to the base salary, as part of our Total Rewards program, Exelixis offers comprehensive employee benefits package, including a 401k plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Employees are also eligible for a discretionary annual bonus program, or if field sales staff, a sales-based incentive plan. Exelixis also offers employees the opportunity to purchase company stock, and receive long-term incentives, 15 accrued vacation days in their first year, 17 paid holidays including a company-wide winter shutdown in December, and up to 10 sick days throughout the calendar year.\nExelixis is an Equal Opportunity Employer. We are committed to fostering an inclusive environment where everyone can thrive. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy (including lactation, childbirth, or related medical conditions), sexual orientation, gender identity, age (40 and over), national origin or ancestry, citizenship or immigration status, physical or mental disability, genetic information (including testing and characteristics), veteran status, uniformed servicemember status, or any other characteristic protected by applicable federal, state, or local law. We are also committed to providing reasonable accommodations to qualified individuals with disabilities, unless undue hardship and/or a direct threat to the health and/or safety of the individual or others would result.\nIf you have a disability and need an accommodation in relation to the recruiting process, please email us at: .\nExelixis is an E-Verify employer.\nWORKING CONDITIONS:\nOur office is a modern space that fosters collaboration and creativity. Teams work closely together, sharing ideas and solutions in a supportive atmosphere. We provide all necessary equipment, including dual monitors and ergonomic chairs, to ensure a comfortable workspace.\nDISCLAIMER:\nThe preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. 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