<div class="content-intro"><div><strong>About Apogee Therapeutics</strong></div> <div> <p>Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally.</p> <p>Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee’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, Apogee is seeking to achieve 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.</p> <p>We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: <u>C</u>aring, <u>O</u>riginal, <u>R</u>esilient and <u>E</u>goless and a commitment to refusing to stop at “good enough”.</p> If this sounds like you, keep reading!</div> <p> </p></div><div class="section page-centered" data-qa="job-description"> <div><strong>Role Summary</strong></div> </div> <div class="section page-centered" data-qa="closing-description"> <p>We are seeking an experienced and motivated medical writer who is responsible for providing clinical and regulatory document support and advanced medical writing expertise to cross-functional teams, ensuring the successful and timely preparation of high-quality documents. This individual will also participate in the development and maintenance of document templates, style guides, and standard operating procedures to ensure consistency and quality across documents and will represent Medical Writing at various team meetings. This position reports to the Director of Medical Writing.</p> <p><strong>Key Responsibilities</strong></p> <ul> <li>Collaborates with cross-functional teams to prepare, review, and edit high-quality, scientifically accurate, and submission-ready documents including, but not limited to: protocols, investigator’s brochures, clinical study reports, briefing documents, Module 2 summary documents, and other clinical and regulatory documents.</li> <li>Communicates deliverables needed, writing process, and timelines to team members, and holds team members accountable to agreed-upon document milestones.</li> <li>Negotiates with functional areas regarding deliverables and timelines to meet conflicting demands, removing barriers and using creativity to ensure teams achieve document-related project goals</li> <li>Ensures compliance with relevant regulatory guidelines, industry best practices, and ethical standards in medical writing and communication.</li> <li>Maintains document templates, style guides, and best practices to ensure consistency and quality in written materials.</li> <li>Oversees the planning, coordination, and execution of medical writing projects by external vendors and consultants to ensure milestones are met and resources are allocated efficiently.</li> <li>Leverages AI-enabled tools to enhance efficiency and quality of medical writing deliverables while maintaining scientific rigor and regulatory compliance.</li> <li>Helps define and implement best practices for the responsible use of AI within medical writing workflows.</li> <li>Provides guidance to less experienced medical writers and external vendors.</li> </ul> <p><strong>Ideal Candidate</strong></p> <ul> <li>Bachelors in science (advanced degree is a plus), with 8+ years of experience in medical writing in the pharmaceutical or biotech industry.</li> <li>Ability to understand, critically analyze, and interpret data and summarize complex results in an unambiguous, concise, and scientifically accurate manner</li> <li>Well-developed interpersonal and communication skills, with experience interacting with and influencing people, and building strong, positive relationships</li> <li>Proven organizational skills and the ability and flexibility to work across a variety of teams and manage multiple competing priorities in a fast-paced startup environment</li> <li>Experience with independently authoring a range of scientific documents and the ability to oversee such authoring done by third parties</li> <li>Detail-oriented, with exceptional organizational and project management skills</li> <li>Proficient in using scientific writing tools (eg, Microsoft Office suite, document management systems, reference management software) and ability to quickly learn new software applications.</li> </ul> <p>The anticipated salary range for candidates for this role will be $160,000-$180,000 / year. 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. </p> </div><div class="content-conclusion"><p> </p> <div><strong>What We Offer </strong></div> <div> <ul> <li>A great culture, grounded in our C.O.R.E. values: <u>C</u>aring, <u>O</u>riginal, <u>R</u>esilient and <u>E</u>goless</li> <li>Opportunity to work in a fast-paced, highly dynamic environment where you help shape the culture and company, wear multiple hats, and learn quickly</li> <li>Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits</li> <li>We provide competitive time off, including three weeks PTO, two one-week company-wide shutdowns a year and dedicated paid sick leave</li> <li>Commitment to growing you professionally and providing access to resources to further your development</li> <li>Apogee offers regular all team, in-person meetings to build relationships and problem solve</li> </ul> </div> <div> </div> <div>E-Verify Participation: As part of the I9 verification of authorization to work in the US, Apogee participates in E-Verify. To learn more about E-Verify please review this <u><a class="postings-link" href="https://www.e-verify.gov/sites/default/files/everify/images/manuals/EVParticipationPoster.JPG">poster</a>.</u></div> <div> </div> <div>A<em>pogee Therapeutics is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.</em></div> <div> </div> <div><em>To review our privacy policy, <a href="https://apogeetherapeutics.com/privacy-policy/">click here</a></em></div> <div> </div> <div><em>It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.</em></div> <p> </p></div>