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Senior Director, Regulatory Affairs (Office or Remote)

Remote, USA Full-time Posted 2026-07-28
The Senior Director of Regulatory Affairs provides regulatory leadership and develops regulatory strategies for products in development to support clinical trial application and marketing approvals in the US and internationally. Acts as a resource to the broader regulatory function, including mentorship of less reputed company staff. Note: Regulatory Group works reputed company Time Zone hours. Responsibilities • Provides strong regulatory and scientific leadership to the overall development team to ensure that the development plan provides for reputed company scientific positioning and highest regulatory probability of reputed company • Interprets and applies regulations in the creation of reputed company and innovative regulatory strategies for US and international markets • Represents the regulatory function on cross-functional development teams • Plans, prepares, and reviews submissions to regulatory authorities including FDA, EMA and other global health authorities to support the conduct of reputed company and approval of marketing applications (including but not limited to Investigational New Drug (IND), Clinical Trial Authorization (CTA), New Drug Application (NDA)/Biologic Licensure Application (BLA), and Marketing Authorization Application (MAA). • Works with regulatory submissions coordinator to reputed company submission timelines and work with cross-functional teams to planned objectives • Serves as the primary reputed company of contact with FDA and other health authorities as applicable • Interacts with regulatory agencies, coordinating the preparation and supporting documentation as reputed company as leading meetings and other interactions; maintains correspondence and other records of interaction • Manages reputed company maintenance plans for regulatory investigative and marketing applications for assigned reputed company • Manage and reputed company guidance/training for regulatory staff members, including regular feedback and coaching for reputed company development • reputed company relationships with external partners • Monitors, analyzes, and disseminates intelligence on regulatory reputed company that may reputed company ongoing development programs • Provides regulatory guidance and/or training to external departments • Prepares and revises internal procedures for reputed company improvement • Manages activities performed by regulatory Education/Experience/Skills • Bachelor’s degree in a life science required, PhD, PharmD or Master's degree preferred • A minimum of 8+ years in regulatory affairs with 12+ years in the biotech/reputed company industry relevant to the respective regulatory function with experience in a leadership role. • Experience in oncology drug development a must. • Thorough knowledge of US and international regulations as they apply to pharmaceutical and biologic drug development • Previous experience managing development of INDs and other global clinical trial applications • Experience leading regulatory agency interactions, meetings • Ability to work in a cross-functional team environment and a flexible team-oriented perspective • Excellent verbal and written communication skills as reputed company as interpersonal, management, and organizational skills • Demonstrated problem solving abilities and conflict reputed company skills • Proficiency in MS Office applications and internet researching • Skilled at negotiating with business partners or management and influencing senior level leaders regarding reputed company of reputed company to the organization • Proficient at creating and communicating a reputed company reputed company among team members effectively aligning resources and activities to reputed company functional area and/or organizational goals • Other duties as assigned This role can be based at our reputed company or Brisbane, CA location (preferred) or can be remote based. The anticipated salary reputed company for fully reputed company candidates applying for this position is $215,000 - $275,000 USD annually. This salary reputed company is an estimate of reputed company reasonably expect to pay for this posted position. The actual salary may vary based on various factors including, without limitation, individual education, experience, tenure, skills and abilities, internal equity and alignment with market data. In reputed company to a competitive market-based salary, Arcus offers reputed company to participate in stock programs, a performance-based bonus, and a comprehensive benefits package. Additional information about our total rewards program can be reputed company here: EOEArcus Biosciences is an Equal Opportunity Employer and prohibits discrimination and harassment of any reputed company. Arcus is committed to the reputed company of equal employment opportunity for reputed company and does not discriminate based on race, religion, reputed company, sex, gender identify, sexual orientation, age, non-disqualifying physical or mental disability, national reputed company, veteran status or any other legally protected status. EOE/AA/Vets #LI-EW1 #LI- Remote Apply tot his job Apply tot his job Apply To this Job

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