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[Remote] Senior Manager, Regulatory Affairs Project Management

Work from home Full-time role Hiring

Note: The job is a remote job and is open to candidates in USA. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets. The Senior Manager, Regulatory Affairs Project Management will optimize planning, execution, and tracking of development-stage global regulatory activities, ensuring alignment with regulatory, global development, and technical operations objectives.

Responsibilities

  • This role blends regulatory expertise with advanced project management skills, developing complex plans to enable successful Regulatory submission activities and ensuring cross-functional integration across regions
  • Track and coordinate timelines and deliverables to support complex regulatory submission activities (IND/CTA/BLA/NDA/MAA) across multiple regions, as well as responses to queries and correspondence with subject matter experts
  • Work with the Regulatory team to translate strategic regulatory vision into actionable project plans, ensuring all cross-functional activities are coordinated and delivered on time
  • Organize and facilitate cross-functional meetings to coordinate, plan, and track submission activities, driving accountability and alignment among stakeholders worldwide
  • Monitor CTA/IND submission status across assigned projects
  • Support strategic planning and risk mitigation efforts related to regulatory activities, including portfolio level analyses that identify resource bottle necks across all programs and studies
  • Support evaluation, implementation, and use of project management tools (especially Smartsheet); define methodologies and reporting frameworks
  • Design and maintain Smartsheet sheets, reports, dashboards, and forms related to regulatory activities and ensure integration with program plans
  • Troubleshoot and enhance PMO solutions, support system updates and new capabilities
  • Demonstrate critical thinking and initiative to improve PM practices

Skills

  • Bachelor's degree in life sciences, pharmacy, chemistry, or related field
  • 5+ years of experience with at least 3+ years of project management experience in pharmaceutical or biotech industry is preferred
  • Experience with planning IND/CTA regulatory submissions required
  • Familiarity with components of regulatory submissions is required
  • Experience planning BLA/NDA/MAA submissions is required
  • Familiarity with CRO operations and global regulatory requirements for clinical trial applications
  • Experience supporting global interventional clinical studies and CTA submissions
  • Hands-on Smartsheet experience; Smartsheet Core Product Certification or equivalent desirable
  • Proficiency in project management tools (Smartsheet, ThinkCell, PowerPoint, Excel, SharePoint, Office Timeline Pro). Familiarity with regulatory systems (Veeva RIM) preferred
  • Knowledge of biotech processes, scientific terminology, drug development concepts
  • Proactive and structured approach to problem-solving, with ability to think cross-functionally and in multiple timeframes, and to distill into actionable plans/solutions
  • Strong organizational, communication, and problem-solving skills with the ability to manage multiple priorities and meet deadlines
  • Ability to work independently and thrive in a dynamic environment
  • Team player that contributes valuable ideas and feedback and can be counted on to meet commitments
  • Position requires up to 20% travel; this includes mandatory in person attendance to company All-Hands meetings held twice a year, additional travel may be required to attend key meetings, typically held at the Apogee San Francisco or Boston offices

Benefits

  • Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits
  • We provide competitive time off, including three weeks PTO, two one-week company-wide shutdowns a year and dedicated paid sick leave
  • Commitment to growing you professionally and providing access to resources to further your development
  • Apogee offers regular all team, in-person meetings to build relationships and problem solve

Company Overview

  • Apogee Therapeutics is a biotechnology company that offers therapies for immunological and inflammatory disorders. It was founded in 2022, and is headquartered in San Francisco, California, USA, with a workforce of 201-500 employees. Its website is https://apogeetherapeutics.com/.
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