Dianthus Therapeutics, Inc.

Manage end-to-end cold-chain logistics and inventory control for biologics across global manufacturing networks. | Requires 5+ years in biopharmaceutical cold-chain logistics, experience with APAC/EU inbound freight, GxP compliance, and relevant certifications. | Job Description: • Execute high-value, end-to-end cold-chain logistics for biologics, focusing heavily on APAC, EU, and US based CRO/CMO/CDMO inventory management. • Responsible for global transportation of drug substance, drug product, and various sample and stability materials. • Maintain tight inventory control over large molecule drug substance, drug product, and other materials and components across a fragmented external manufacturing network. • Anticipate and mitigate cross-border transit risks; ensure strict GxP and temperature compliance, optimize international transportation lanes, and streamline customs clearance. • Build effective partnerships with key stakeholders across a range of functions, including CMC and GMP manufacturing, Analytical Development, Quality Assurance, Discovery, and external service providers, to ensure delivery of materials to support all product programs. • Partner with 3PLs to ensure delivery timeline adherence and resolve customs holds and delays. Requirements: • Bachelor’s Degree in Supply Chain Management, Logistics, Business Administration, Life Sciences, or a related Life Sciences field. • At least 5 years of biopharmaceutical, pharmaceutical, or medical device cold-chain logistics, with a focus on biologics or large-molecule products. • At least 2 years of direct experience managing inbound freight forwarding from APAC and EU countries into the United States. Strong knowledge of global trade compliance and biologics import/export requirements and GxP regulations. • Strong knowledge of thermal packaging and temperature monitoring technology. • Advanced experience in Excel and basic experience utilizing ERP systems (Oracle/Oracle NetSuite, SAP, etc.), Laboratory Information Management Systems (LIMS), and Warehouse Management Systems (WMS). • Certifications such as Certified Supply Chain Professional (CSCP) and Certified in Logistics, Transportation and Distribution (CLTD), and/or training in IATA Dangerous Goods (for dry ice / LN2 shipments) are highly preferred. • Ability to translate technical logistics data cleanly to Technical Operations and Finance teams. Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams. • Skilled at evaluating complex transit data, trade lane costs, and warehouse capacity constraints. • Strong ability to forecast supply chain bottlenecks, geopolitical disruptions, and build robust contingency routes for high-value biological cargo. • Ability to effectively collaborate with APAC and EU partners across significantly different time zones. Benefits: • We are building a culture of individuals who hold our core principles at the center of our operations, with the goal to elevate the care of our patients’ lives. • Open to you working remotely.

Lead and execute medical publication strategies, develop medical communications materials, manage a publications team, and engage with key scientific stakeholders. | Advanced scientific degree (PhD, MD, PharmD), experience in publication planning and medical communications, clinical trial and regulatory knowledge, leadership skills, and excellent communication. | About Us Dianthus Therapeutics is a publicly traded, clinical-stage biotechnology company dedicated to designing and delivering novel, best-in-class monoclonal antibodies with improved selectivity and potency. Based in New York City and Waltham, Mass., Dianthus is comprised of an experienced team of biotech and pharma executives who are leading the development of next-generation antibody complement therapeutics, aiming to deliver transformative medicines for people living with severe autoimmune and inflammatory diseases. To learn more, please visit www.dianthustx.com and follow us on LinkedIn. About the Role The Senior Director, Publications and Medical Communications will play a pivotal role in shaping and executing the company's medical communication strategy. Reporting to the SVP, Global Medical Affairs, you will lead the development and dissemination of high-quality scientific and medical information to support the company's products and pipeline. The role requires strategic vision, operational excellence, and the ability to collaborate cross-functionally in a fast-paced, start-up environment. This is an exciting opportunity to join a phase II/III biotech company. We are building a culture of individuals who hold our core principles at the center of our operations, with the goal to elevate the care of our patients' lives. We are open to you working remotely. Key Responsibilities Publications Planning and Execution: • Develop and implement a comprehensive publication strategy aligned with corporate and medical objectives. • Oversee the preparation, review, and submission of manuscripts, abstracts, posters, and presentations for peer-reviewed journals and scientific congresses. • Ensure publications adhere to ethical and compliance standards (e.g., ICMJE guidelines, GPP). Medical Communications: • Lead the development of medical communication materials, including slide decks, FAQs, and evidence-based responses for medical science liaisons (MSLs). • Drive the creation of educational tools and materials to support internal and external stakeholders. • Collaborate with cross-functional teams to develop and execute medical content for advisory boards, investigator meetings, and symposia. Team Leadership and Collaboration: • Build and manage a high-performing publications and medical communications team, including internal staff and external vendors. • Partner with Clinical Development, Regulatory, Commercial, and other key teams to ensure alignment of communication strategies with business objectives. • Provide strategic input to clinical trial design and data analysis to ensure impactful dissemination of study results. Compliance and Quality: • Ensure all publications and medical communications are accurate, balanced, and consistent with regulatory guidelines and company policies. • Maintain a thorough understanding of the competitive landscape and emerging data in the field. Stakeholder Engagement: • Foster relationships with key opinion leaders (KOLs), external experts, and academic collaborators. • Represent the company at scientific and medical conferences and meetings. Experience • Advanced degree in a scientific or medical discipline (PhD, PharmD, MD, or equivalent preferred). • Proven experience in developing and executing publication plans and medical communication strategies. • Strong knowledge of clinical trial design, data interpretation, and regulatory requirements. • Excellent leadership and team management skills. • Exceptional written and verbal communication skills, with the ability to translate complex scientific data into clear, concise messaging. • Ability to thrive in a fast-paced, entrepreneurial environment and adapt to evolving priorities.