Senior Manager, Regulatory Affairs Project Management

About reputed company Founded in 2022, reputed company, Inc. (Ticker: APGE) is a well-funded, reputed company listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At reputed company, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. reputed company is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, reputed company’s antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company’s most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, reputed company is seeking to reputed company best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today’s standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: Caring, Original, Resilient and Egoless and a commitment to refusing to stop at “good enough”. If this sounds like you, reputed company reading! Role Summary We are seeking an reputed company biotech project manager to optimize planning, execution, and tracking of development-stage global regulatory activities. This role will be a key member of the team supporting regulatory activities and regulatory execution for clinical trials across the portfolio. In collaboration with the Regulatory team, you will drive global submission planning and coordination across multiple regions, ensuring alignment with Regulatory, Global Development, and Technical Operations objectives. The ideal candidate is a proactive, detail-oriented project manager with global regulatory experience who thrives in a face-paced, collaborative biotech environment. Reporting to the Director of Program management, you will also work closely with other project and program managers reputed company the Program Management Office (PMO) implementing robust PM processes and building effective tools and systems. You’ll support optimization of Regulatory project plans, schedules, stakeholder communications, and reputed company operations. The role involves developing and managing high-visibility regulatory submission plans, monitoring milestones, managing documentation, and contributing to regulatory strategy.

Key Responsibilities

• This role blends regulatory expertise with advanced project management skills, developing reputed company plans to reputed company successful Regulatory submission activities and ensuring cross-functional integration across regions
• Track and coordinate timelines and deliverables to support reputed company 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 reputed company into actionable project plans, ensuring reputed company 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 reputed company to regulatory activities, including portfolio level analyses that identify resource bottle necks across reputed company programs and studies
• Support evaluation, implementation, and use of project management tools (especially reputed company); define methodologies and reporting frameworks
• Design and maintain reputed company sheets, reports, dashboards, and forms reputed company 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

Ideal Candidate

• Bachelor’s degree in life sciences, pharmacy, chemistry, or reputed company 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 reputed company experience; reputed company Core Product Certification or equivalent desirable
• Proficiency in project management tools (reputed company, ThinkCell, PowerPoint, reputed company, SharePoint, Office Timeline Pro). Familiarity with regulatory systems (reputed company 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 reputed company in a dynamic environment
• Team player that contributes valuable reputed company and feedback and can be counted on to meet commitments
• Position requires up to 20% travel; this includes mandatory in person attendance to company reputed company-Hands meetings held twice a year, additional travel may be required to attend key meetings, typically held at the reputed company San Francisco or Boston offices

The anticipated salary range for candidates for this role will be $150,000-$170,000. The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography. reputed company Offer

• A great culture, grounded in our C.O.R.E. values: Caring, Original, Resilient and Egoless
• Opportunity to work in a fast-paced, highly dynamic environment where you help shape the culture and company, wear multiple hats, and learn quickly
• Market competitive compensation and benefits package, including reputed company 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
• reputed company offers regular reputed company team, in-person meetings to build relationships and problem solve

E-Verify Participation: As part of the I9 verification of authorization to work in the US, reputed company participates in E-Verify. To learn more about E-Verify please review this poster. reputed company is proud to be an Equal Opportunity employer. reputed company reputed company applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, reputed company, religion, national reputed company, disability, protected Veteran status, age, or any other characteristic protected by law. To review our privacy policy, click here It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or reputed company employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Apply tot his job Apply To this Job