• Develop statistical and machine learning models with a modeling & simulation lens to help quantify and reduce future uncertainty across various scenarios • Build well-structured and understandable code to enable smooth collaboration across the team and successful model deployment • Serve as a trusted technical expert who can offer informed guidance on methodology or technology decisions and communicate core requirements to our technology teams • Mentor junior team members by providing guidance on best practices in data science • Stay abreast of industry trends and methodologies and contribute innovative ideas to drive business value

Medical Scientist - Respiratory Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. • We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities • Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans. • Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. • Authors medical data queries and reviews query responses, approves query closure in association with Medical Director. • May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed. • Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed. • Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review. • Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the project leads in a timely manner. • Attends at Trusted Process meetings and may participate in internal and external audits. • Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology. • Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans. At  Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements. Salary Range: $67,700.00 - $115,100.00 The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Medical Scientist - Cardiovascular Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: Why Syneos Health • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. • We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities • Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans. • Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. • Authors medical data queries and reviews query responses, approves query closure in association with Medical Director. • May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed. • Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed. • Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review. • Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the project leads in a timely manner. • Attends at Trusted Process meetings and may participate in internal and external audits. • Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology. • Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans. At  Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements. Salary Range: $67,700.00 - $115,100.00 The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

O(a) Cientista de Pesquisa de Produção é responsável pelo planejamento, execução, análise e aplicação de atividades de pesquisa de produção em campo, com foco em producibilidade, qualidade, confiabilidade e eficiência de custos na produção de sementes. Esta posição atua em estreita colaboração com Desenvolvimento de Produtos, Seed Production & Supply Chain e Operações, gerando insights baseados em dados que suportam decisões de avanço de produto, gestão de risco de parentais e melhoria contínua dos sistemas de produção, alinhados aos princípios End‑to‑End. Principais Responsabilidades Execução de Pesquisa de Produção - Planejar e executar ensaios de pesquisa de produção com foco em caracterização de parentais, otimização agronômica e mitigação de riscos de producibilidade. - Garantir que os experimentos sejam conduzidos de acordo com protocolos aprovados, cronogramas estabelecidos e padrões de segurança. - Gerenciar atividades de pesquisa em múltiplas localidades e safras, alinhadas às prioridades regionais de produção. Caracterização de Parentais & Suporte à Producibilidade - Desenvolver e interpretar dados de caracterização de parentais para suportar decisões de avanço de produto, posicionamento produtivo e avaliação de risco. - Colaborar com equipes de Desenvolvimento de Produtos e SPRC para converter resultados de pesquisa em diretrizes claras de producibilidade. - Apoiar iniciativas voltadas à redução da complexidade produtiva, custos e riscos de execução. Análise de Dados & Suporte à Decisão - Analisar e resumir conjuntos de dados agronômicos e produtivos complexos para apoiar decisões técnicas e operacionais. - Preparar relatórios, sumários e apresentações para equipes técnicas e liderança. - Garantir a precisão, consistência e integridade dos dados de pesquisa e conclusões. Implantação de Melhores Práticas - Apoiar a implantação e adoção de práticas agronômicas e procedimentais aprimoradas nos ambientes de produção de sementes. - Trabalhar em parceria com Operações e Supply Chain para permitir a execução eficaz das recomendações de pesquisa no campo. - Contribuir para iniciativas de melhoria contínua dentro da área de Pesquisa de Produção. Colaboração Multifuncional - Atuar de forma colaborativa com Operações, Seed Production & Supply Chain, Desenvolvimento de Produtos, Qualidade e Comercial. - Contribuir tecnicamente em projetos multifuncionais que impactam o desempenho da produção de sementes. - Comunicar resultados e recomendações de pesquisa de forma clara e adequada a diferentes públicos. Pessoas & Desenvolvimento de Capacidades - Fornecer orientação técnica e suporte diário a Técnicos de Pesquisa de Produção e equipes temporárias, quando aplicável. - Promover conformidade com padrões de segurança, qualidade e governança de dados. - Apoiar o desenvolvimento da capacidade técnica da organização de Pesquisa de Produção. Requisitos Obrigatórios Formação - Graduação em Agronomia, Ciências Agrárias, Ciência de Plantas, Genética ou áreas relacionadas - Pós‑graduação (Mestrado ou Doutorado) desejável - Inglês é desejado Experiência - Experiência em ambientes de produção de sementes, pesquisa agronômica ou P&D agrícola. - Experiência com experimentação de campo e análise estatística e aplicada de dados. - Vivência em ambientes multifuncionais ou estruturas matriciais com experiência de, no mínimo, 5 anos em sementes Competências Essenciais - Conhecimento aplicado em agronomia e produção de sementes - Habilidade analítica e resolução de problemas - Interpretação de dados e elaboração de relatórios técnicos - Colaboração e engajamento com stakeholders - Mentalidade de melhoria contínua - Comunicação técnica eficaz #LI-Remote Corteva Agriscience is an equal opportunity employer. We are committed to embracing our differences to enrich lives, advance innovation, and boost company performance. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, military or veteran status, pregnancy related conditions (including pregnancy, childbirth, or related medical conditions), disability or any other protected status in accordance with federal, state, or local laws.