• Provides medical oversight of assigned clinical studies in the duty as a medical monitor • Often serves as primary medical contact for customers for assigned clinical studies • Responsible for protocol design and development, upon request • Provides medical and therapeutic input to Study Start Up, Feasibility, and Subject Identification efforts • Presents identified trends and issues to customers and project team members

Role Description Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you’ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs. The Director, Medical Portfolio Strategy and Solutions, Population Health is accountable for leading development of the medical engagement strategy for US IDN Health System & Population Health, organized customers and other population health stakeholders, to include: - Insight generation - Population health initiatives - Scientific content and educational program development An important element of this role is to drive innovation with medical initiatives and simplify and enhance the customer engagement experience through impactful and personalized content tailored to organized customer needs and preferences. Main Responsibilities - Develop the medical engagement strategy, including educational initiatives and related content, tools and resources, intended for payer and population health decision makers and other organized customers. - Develop population health related initiatives aimed at helping population health stakeholders improve quality of care and health outcomes, in collaboration with relevant internal stakeholders. - Develop and implement non-CME medical education programming, including through partnerships with professional societies such as AMCP and ASHP. - Drive innovation with customer engagement approaches by leveraging AI, digital technologies, and emerging platforms to enhance scientific communications and create more personalized, impactful interactions and a consistent customer journey. - Serve as therapeutic area subject matter expert for scientific engagement with strategic accounts, develop and deliver educational programming for population HCDMs, and represent MVO function at payer and scientific congresses. - Ensure content strategy and materials are aligned with TA scientific communication plans and Specialty Care Market Access stakeholders. - Lead and coordinate Early Scientific Dialogue consultancies with organized customers, collaborating closely with internal stakeholders to ensure insights shared with relevant stakeholders are pulled through into integrated evidence generation plans. - With support of project management, manage content workflow from MedHub and Vendor into appropriate review process and content management library. - Coordinate with Field Team leaders and Medical Excellence roles to optimize content usage, customer experience, and employee experience. - Contribute to the evolution of medical omnichannel engagement by building and enabling capabilities that facilitate a fully integrated channel content strategy. - Leverage AI-powered solutions and digital resources to enhance data analysis, content personalization, and customer engagement effectiveness. - Leverage customer insights, market research and multiple data sources to identify innovative educational and content opportunities. - Collaborate with Global Sci Com, Global and US medical teams, Med Hub, and vendors to ensure synergies with content development, build cross-portfolio consistency with MVO team content and resources, and partner across business units with medical outcomes functions on common above brand resources. - Develop and manage the payer medical consultant panel, insight generation initiatives and analytics, and other advisory panels or market research. - Work with Global medical publications and TA stakeholders to develop relevant local publications directed at US payer and population HCDM audience. - Partner with Global Medical Information to develop specific healthcare economic information SRDs relevant for US payer and population health stakeholders. - Collaborate with HEVA to provide input and medical review of economic models, BIMs, dossiers, and patient estimator tools. - Collaborate with Independent Medical Education to support the review of payer-related educational grant requests and opportunities for population health and payer HCDM-focused education. - Collaborate with Public Affairs and TA medical units to coordinate opportunities to support scientific engagement with PAG Leadership. - Participate in and actively contribute to integrated evidence generation planning process to ensure the US payer and population HCDM voice is included in US evidence gap analysis. - Contribute to organized customer evidence generation partnerships as key member of project team, serving as TA and Strategy subject matter expert with customer. - Serve as medical partner to Value & Access brand leads and other stakeholders to provide input on product value proposition, ensure alignment on customer engagement plans, and support account team training as appropriate. - Facilitate field MVO team integration and alignment with key stakeholders including TA medical unit, Value & Access, and HEVA, including representation with medical brand planning across TA teams. - Provide comprehensive field team support and training, including leading the development of training materials, facilitation of TA and product training and certifications, and management of proactive scientific exchange training requirements. - Serve as medical reviewer for payer facing resources, as requested and when appropriate. - Develop performance and impact measures for prioritized field medical initiatives including tools to capture insights on customer receptivity to scientific content and value proposition. - Conduct US tiering of non-HCP payer and HEOR consultants for Specialty Care business unit. - Lead a team of MVO advisors that provide field input and customer insights to inform the development of medical initiatives, content, and resources, in partnership with field leadership advisor and other key stakeholders. - Plan and manage program budgets. - Ensure compliance with all local regulations. Qualifications - Advanced degree in healthcare or related scientific discipline (PharmD, MD, PhD, MS, etc.) required; MBA or relevant business background a plus. - Relevant experience in a specialty care therapeutic area of focus (immunology, neurology, oncology, rare blood disorders). - Deep understanding of US healthcare delivery dynamics across health systems, payers, providers, and other key influencers. - At least 3 years of experience in the pharmaceutical industry. - At least 2 years of experience in medical strategy, content development and design, and scientific communications. - Strong business acumen. Professional Qualifications and Skills - Experience with omnichannel communications and scientific content development including storytelling, creativity, design, written, verbal and presentation skills. - Deep knowledge of US healthcare delivery landscape and defining opportunities for scientific partnerships with key stakeholders to improve health outcomes. - Ability to leverage adult learning principles to maximize content effectiveness. - Strong planning and project management skills, with ability to prioritize and work independently on simultaneous projects. - Analytical and detail oriented, pragmatic in solving problems. - Proficiency in Microsoft O365 office suite applications as well as content creation software. - Knowledge of AI applications and digital technologies for enhancing scientific communications and customer engagement. - Proven ability to work in a fast-paced, change-oriented environment. - Willingness and ability to lead or facilitate collaboration across functions, global and local, and within Commercial team. - Commitment to policy, procedure, and precise documentation. - Respect for diversity of thought. - Awareness and understanding of content management systems and processes (Veeva CRM, CLM, PromoMats, etc.). Local Specificities - Travel approximately 20-25% required for field-related responsibilities, internal meetings, appropriate engagement with internal stakeholders, and participation in relevant congresses and professional meetings. - Field-based position with therapeutic area subject matter expert responsibilities. - Dedicated leads defined by therapeutic area with defined responsibility for above brand and cross-portfolio initiatives and resources. - Requires deep understanding of US healthcare delivery dynamics and strong expertise in scientific content development, omni-channel and digital engagement and project management. - Position serves as key partner for integrating with TA medical units, Value & Access TA and brand, and other key internal stakeholders. Benefits - Bring the miracles of science to life alongside a supportive, future-focused team. - Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. - Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. - Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

• Manage the Health Plan Medical Directors • Provide clinical support for the Health Management Utilization Management, Care Management and Quality teams • Drive the development, promotion and delivery of high quality, evidence-based utilization and care management programs and processes • Lead programs and reviews to support effective medical expense management, medical quality programs and outcomes, and programs to manage medical utilization trends such as inpatient, Emergency Department, Site of Care, pharmacy and radiology • Achieves defined clinical outcomes, affordability goals and growth targets • Works closely across the HP to ensure compliance with government program regulations, including management of clinical appeals and grievances with sound clinical evidence and advice • Works closely with the Medical Directors and the Director of Medical Economics to devise analytic approaches that support and measure strategic development and sound clinical programs • Provides clinical insight into data to assist in development of and measurement of tailored interventions that address clinical trends and opportunities • Develops key strategies to address opportunities in medical expense management • Identifies opportunities for improvement in the quality of care that create competitive advantage for Martin’s Point as it relates to the health of populations served • Accountable for appropriate Utilization Management processes • Assists and provides clinical input into the evolution of care/utilization management, quality, and pharmacy related programs • Contributes to and advises in product design and the Medicare bid processes • Contributes to and advises in areas of clinical integration as it relates to risk adjustment • Serves as a central HP leader aligning medical, clinical, and operational functions to achieve seamless and thorough solutions related to Medical and Payment Policies • Actively engages with quality, network, and compliance teams to help drive performance

Role Description The Medical Director role works closely with the Executive Director, Clinical Development, and is responsible for protocol design and scientific oversight of clinical research studies involving new or marketed drugs. S/he will contribute to the clinical development and regulatory strategy for assigned assets, and will also be accountable for the design, execution, oversight, monitoring and report of clinical trials. This position reports into the Executive Director in the Global Clinical Development group within the Clinical Development and Operations organization. This position can be remote within the US Responsibilities - Lead or contribute to the development and updates to the global clinical development plan. - Work closely with Operations and vendor to identify and/or vet sites for clinical trial participation. - Design patient-centered clinical protocols that support strategic objectives, are feasibly conducted, and support efficient recruitment to meet program timelines. - Represent clinical development on study teams, collaborating closely with clinical operations and team members in identifying clinical study issues, barriers to execution, and developing sound strategic solutions with partners of the study team to ensure timely resolution. - Provide clinical input to clinical study teams for key documents, including informed consent, data review plans, medical monitoring plans, statistical analysis plans, clinical review forms, case report forms, data edit checks. - Participate in design and conduct of Investigator Meetings for clinical trials. - Monitor study conduct to ensure efficient recruitment, high quality of data and fidelity to protocol, and to minimize compliance and quality risks to enable a decisive readout. - In collaboration with biostats and safety, interpret efficacy and safety data from clinical trials and author CSR. - Directly monitor and provide oversight to CRO medical monitors, depending on the study execution model, to ensure patient safety and high-quality trial conduct. - Monitor study safety and provide input to safety narratives and reports. - Collaborate with regulatory affairs on the clinical development and regulatory strategy to result in successful global submissions and approvals, integrating clinical, regulatory, market access and commercial considerations. - Author and edit regulatory documents, including but not limited to briefing packages, response documents, and submission dossiers. - Coauthor abstracts and publications and review IIS proposals as requested. - Build strong relationships with medical affairs and external thought leaders in supporting clinical development objectives. - Plan and execute advisory boards to support clinical development objectives. - Build strong relationships with patient advocacy groups to support patient-centered clinical development across all phases of development. - Collaborate with medical affairs and commercial organization on life cycle management opportunities that generate value for the asset. - Participate in due diligence projects as requested to support assessment of external assets. Qualifications - MD, DO, or MRCP. - 2-4 years experience in clinical development in a biotech or pharma setting. - Relevant clinical experience in women’s health, dermatology, or pediatric development is preferred. - Investigators with substantial clinical trial leadership or relevant research experience in an academic setting will also be considered. - Familiarity with ICH, GCP, clinical trial execution including medical monitoring processes. - Stays up to date with and uses relevant regulatory guidances, precedents, scientific literature and therapeutic landscape to anticipate risks and mitigations to clinical trial design and regulatory strategy. - Critically analyzes data quality and interpretation. - Collaborates with a one team mindset, fosters diverse perspectives, and leads matrixed team through complex decisions. - Functions with high level of independence. - Able to prioritize and deliver work, and adapt to changing corporate priorities, in a rapidly evolving environment. - Possess a high degree of integrity and personal ethics. - Strong written and oral communication skills. - Fluent in written and spoken English. - Travel may be required to support clinical trials or external engagement. Benefits - Retirement savings plan. - Paid vacation and holiday time. - Paid caregiver/parental and medical leave. - Health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Company Description Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women’s Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman.