<p>Phathom Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of gastrointestinal (GI) diseases. With exclusive rights in the United States, Europe, and Canada to vonoprazan-a first-in-class potassium-competitive acid blocker (PCAB)-Phathom is working to transform the treatment of acid-related disorders.</p> <p>Our current portfolio includes:</p> <ul> <li> <p>VOQUEZNA (vonoprazan) tablets, approved for the treatment of heartburn associated with Non-Erosive GERD, as well as the healing and maintenance of healing of Erosive GERD</p> </li><li> <p>VOQUEZNA TRIPLE PAK (vonoprazan tablets, amoxicillin capsules, clarithromycin tablets) and VOQUEZNA DUAL PAK (vonoprazan tablets, amoxicillin capsules), approved for the treatment of H. pylori infection in adults</p> </li></ul> <p>Beyond our commercialized products, we are advancing a pipeline focused on innovative treatments for other acid-related GI disorders, including Eosinophilic Esophagitis (EoE).</p> <p>At Phathom, we are fueled by innovation, driven by purpose, and united by a shared commitment to improving patient outcomes. Our team comprises seasoned GI and industry experts with proven track records of delivering groundbreaking therapies, including anti-secretory agents. Together, we are tackling unmet medical needs and working hard to enhance the lives of patients.</p> <p>We seek motivated, innovative problem-solvers who excel in fast-paced, collaborative environments and are eager to make an impact. At Phathom, you'll find more than a career - you'll join our "Phamily," where employees feel empowered, valued, and inspired to do their best work.</p> <p>In August 2025, we proudly earned the distinction of being Great Place to Work certified, with 91% of surveyed employees affirming that Phathom is an exceptional workplace.</p> <p>Ready to help change the landscape in GI? Join us and be part of something extraordinary.</p> <p>OBJECTIVES</p> <ul> <li>To provide senior-level medical and scientific leadership within the Promotional Review Committee (PRC) and Medical Review Committee (MRC), ensuring strategic, scientifically accurate, and compliant promotional and non-promotional materials. </li><li>To oversee the Medical Information strategy and ensure the development of high-quality, balanced, and scientifically rigorous medical information responses for HCPs and patients. </li><li>To serve as a senior therapeutic-area expert, maintaining deep knowledge of clinical evidence, competitive landscape, treatment guidelines, and unmet needs to inform brand and medical strategy. </li><li>To guide cross-functional teams (Commercial, Legal, Regulatory, R&D) in developing scientifically supportable claims, identifying evidence gaps, and shaping data-generation needs. </li></ul> <p>ACCOUNTABILITIES</p> <ul> <li>Leads Medical Affairs representation in PRC/MRC, providing authoritative medical assessment of claims, references, data relevance, and scientific rigor. </li><li>Ensures promotional materials reflect accurate, balanced, and supportable scientific content and provides proactive recommendations for compliant claim alternatives. </li><li>Oversees Medical Information content development, including standard response letters, escalated inquiries, and cross-functional alignment of medical messaging. </li><li>Partners with Commercial, Regulatory, Legal, and R&D colleagues to support brand strategy, future claim feasibility, and risk-mitigation planning. </li><li>Maintains subject matter expertise in disease state, guidelines, and competitive intelligence to inform internal teams and influence medical strategy. </li><li>Leads medical information and scientific engagement activities at professional congresses, ensuring appropriate training, staffing, and documentation. </li><li>Provides medical training for internal teams (Commercial, MSLs, Medical Affairs) on scientific and promotional standards. </li></ul> <p>EDUCATION & EXPERIENCE</p> <ul> <li>Advanced scientific degree required (PharmD, PhD, MD preferred). </li><li>At least 6 years of Medical Affairs experience, with PRC/MRC involvement preferred. Senior title may be considered based on tenure and experience, including launch strategy or major regulatory milestone support. </li><li>Deep expertise in clinical development, therapeutic guidelines, competitor landscape, and scientific data interpretation. </li><li>Extensive understanding of FDA promotional regulations, OPDP standards, and medical-legal compliance. </li><li>Excellent written and verbal communication skills with the ability to influence cross-functional partners. </li><li>Strong organizational skills and the ability to manage complex workloads and competing priorities. </li></ul> <p>Phathom's Core Values:</p> <ul> <li> <p>Perseverance - With hard work and determination, together we overcome all obstacles</p> </li><li> <p>Humble - We put others first, remain grounded and let our work speak for itself</p> </li><li> <p>Accountable - We are reliable and take personal responsibility in all that we do. We take pride and ownership in our work every day</p> </li><li> <p>Transparent - We say what we mean, debate openly and respectfully, and have no hidden agendas</p> </li><li> <p>Entrepreneurial - We are nimble, agile and embrace innovation. We challenge the status quo, enjoy change and approach problems unconventionally</p> </li></ul> <p>Working at Phathom:</p> <p>At Phathom, we prioritize the total well-being of our "Phamily" members. Our commitment is reflected in a competitive employee benefits package designed to support employees and their families' overall well-being, now and in the future, including:</p> <ul> <li> <p>Highly competitive medical, dental and vision coverage options with low monthly premiums</p> </li><li> <p>Roth & Traditional 401(k) savings plan with annual employer match</p> </li><li> <p>Long-term incentive equity compensation program</p> </li><li> <p>Employee Stock Purchase Plan (ESPP)</p> </li><li> <p>Comprehensive paid leave programs, including:</p> </li><li> <p>16 weeks of paid parental leave for all new parents</p> </li><li> <p>4-week part-time Bridge-Back-to-Work Program</p> </li><li> <p>Hybrid and Flex Working Arrangements</p> </li><li> <p>Unlimited Time Off</p> </li><li> <p>17 paid company holidays in addition to a year-end winter shutdown period</p> </li></ul> <p>Other Benefits:</p> <ul> <li> <p>Annual Fitness & Wellbeing Reimbursement</p> </li><li> <p>Company-provided Life and Accidental Death & Dismemberment (AD&D) insurance</p> </li><li> <p>Company-provided short and long-term disability benefits</p> </li><li> <p>Company-funded HSA plan</p> </li><li> <p>Accident and Hospital Indemnity insurance</p> </li><li> <p>Employee Assistance Program (EAP)</p> </li><li> <p>Employee recognition program</p> </li><li> <p>Employee discounts</p> </li></ul> <p>Annual Base Salary: $210,000 - $240,000</p> <p>Phathom is an equal opportunity employer that is committed to inclusion and diversity and provides equal opportunity for all applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, Veteran status, or other legally protected characteristics.</p> <p>Applicants with a disability who require a reasonable accommodation for any part of the application, interview or hiring process can contact us by sending an email to?careers@phathompharma.com.</p>