Director, Medical Affairs (Nutrition)

Job Summary The Director, Medical Affairs (Nutrition) is responsible for leading and managing medical affairs for approved nutrition products and those in development. Areas of support include Product pre‑launch and launch activities, Product Development, Product Lifecycle management, Business Development, and Post‑Marketing medical affairs strategies. The role collaborates cross‑functionally and globally to ensure corporate goals and objectives are met at the highest levels. It directs the Region’s medical needs for support of drugs and devices on the market, in development, and under evaluation. The Director is responsible for cultivating and maintaining external relationships, especially with Health Care Providers (HCPs) and/or Health Care Decision Makers (HCDMs), to enable comprehensive scientific exchange around disease states and associated Company products. The Director must maintain scientific expertise in the application of treatment guidelines and clinical data as it pertains to disease states and associated Company products, and must be able to communicate complex medical and scientific concepts to a broad range of audiences. The Director will also support execution of medical affairs strategy and activities where and as appropriate. The Director will lead the field clinical education team and ensure that the respective territory engagement plans are effectively executed per defined targets, following compliance rules and the code of conduct, and that relevant medical and scientific insight is routinely shared to optimize the Medical Affairs strategy for the nutrition portfolio. Hiring Details Priority will be given to candidates in the Chicagoland area who are able to regularly work at our Lake Zurich, IL site. This position does not offer visa sponsorship either now or in the future. Salary Range: $185,000–220,000. Position is eligible to participate in an annual bonus plan with a target of 16% of the base salary. Position is eligible to participate in our medium‑term incentive plan. Final pay determinations will depend on various factors, including, but not limited to, experience level, education, knowledge, skills, and abilities. Benefits include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage. Responsibilities Lead the strategic planning, launch, and lifecycle support of nutrition products including high‑risk medications. Lead the development and execution of medical affairs strategy to support successful product launch ensuring alignment with commercial, clinical development, regulatory teams and internal stakeholders. Maintain the highest levels of professional integrity & performance standards by consistently providing high‑quality medical deliverables on time. Maintain a high standard for medical and scientific accuracy, representative of a comprehensive understanding of the medical concept at hand. Maintain a high level of professional expertise by staying abreast of the current medical landscape with regard to key clinical conditions our products support. Identify, engage, and build strong relationships with Key Opinion Leaders (KOLs), influencers in HCP community, scientific experts, and medical societies to support scientific exchange and advocacy. Lead the nutrition team ensuring achievement of compliant and effective healthcare professional interaction for scientific exchange related to disease states and/or associated Company products per predefined engagement plans and targets. Establish and maintain relationships with HCPs and HCDMs to provide scientific exchange related to disease states and/or associated Company products. Represent the company at major medical and scientific conferences; manage planning and coordination of congress activities, including symposia, medical affairs booth presence, and thought leader engagements. Oversee publication planning and execution, including abstracts, posters, manuscripts, and scientific communications, ensuring timely and compliant dissemination of clinical data. Drive medical education initiatives for internal and external stakeholders, including training programs, advisory boards, and peer‑to‑peer education aligned with the product’s scientific platform. Provide scientific leadership and oversight for Investigator‑Initiated Trials (IITs), including review, approval, and ongoing collaboration with investigators. Collaborate cross‑functionally to design and implement company‑sponsored clinical studies to support product differentiation, real‑world evidence generation, cost‑effectiveness analysis, HEOR studies and post‑marketing commitments. Lead and manage a team of medical affairs professionals; provide coaching, development, and performance management to ensure high team effectiveness. Collaborate with Global Medical Affairs in the support of USA‑based clinical trials, both internal and external. Review, develop, and approve clinical summaries in support of NDA 505(b)(2), ANDA, NDA applications. Serve as a medical expert for on‑market parenteral nutrition products, products in development, and potential acquisition targets, providing medical affairs strategies and due diligence for on‑market products and business development opportunities. Responsible for writing and/or review of relevant Standard Operating Procedures (SOPs) pertaining to the role as needed. Job Requirements Medical/clinical professional degree required, such as Licensed Registered Dietitian. Clinical Nutrition knowledge is required. 10+ years of experience in the pharmaceutical industry in a medical affairs or clinical development role required. 3+ years of hands‑on experience in patient care and in hospital and/or clinic and/or home infusion settings is required, with demonstrated expertise in clinical nutrition including experience in managing formula selection for oral nutritional supplement use and tube feeding regimens. 5+ years of clinical experience preferred. 5+ years of direct people management experience with demonstrated ability to develop and lead high‑performing teams. Ability to understand and interpret the regulatory requirements under which drugs and devices are developed, reviewed, and supported after approval. Experience with the clinical drug development process and product launch experience is highly preferred. Scientific research and writing skills required. Ability to critically evaluate the published medical and scientific literature and approve and write comprehensive, medically accurate and scientifically fair‑balanced documents. Position will require travel (20–50%), including overnight stays. A valid US driver’s license and clean driving record are required. Ability to understand and interpret FDA 505(b)2, 505(b)1, 505 (j) submission requirements. Knowledge of PC systems and Microsoft Office Suite (Word, Excel) is required. Additional Information We offer an excellent salary and benefits package including medical, dental, and vision coverage, as well as life insurance, disability, 401(k) with company contribution, and wellness program. Please note that joining our team does not create a guaranteed or permanent employment arrangement. All employment is at‑will, meaning both the employee and Fresenius Kabi have the right to end the employment relationship at any time, in accordance with applicable federal and state laws. Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status. #J-18808-Ljbffr