• Drive the design and timely execution of clinical research plans, including clinical studies and investigator-initiated studies, research projects. • Build relationships with KOLs, consortiums, clinical site staff, and external partners to fill identified data gaps. • Develop clinical project execution timelines and provide status updates to senior management to ensure timely delivery of program milestones. • Drive contracting, including budget approvals, with academic centers and community practices participating in Natera research studies. • Participate in due diligence activities to evaluate external opportunities that support Natera’s business objectives. • Effectively interact with senior members in other functional areas for strategic planning to ensure optimized clinical development in accordance with corporate objectives. • Lead project resource planning, reforecasting, and program milestones. • Manages a team (usually 3-6) working on a variety of routine and complex tasks. • Completes required work independently as well as managing work through direct reports. • Responsible for staffing assigned projects and for the professional development of direct reports. • Makes recommendations to management on matters related to human resources, budget, and department operations. • Identifies, recruits, and hires functional staff. • Ensure that employees are appropriately trained, developed, and coached to comply with study requirements, company policies, and respective agency regulations. • Advocate for and drives timely completion of assigned goals and organizational changes within the organization. • Leads by example to create a positive work environment by encouraging mutual respect, accountability, smart risks, and innovation on a functional and project level. • Offers help, support, and knowledge to drive for success across the organization and company (no silos).

• Responsible for the strategy, external representation, and program leadership for clinical services in high-stakes settings. • Lead the clinical quality approach to client audits, consultant engagement, and longitudinal quality assurance. • Represent Included Health in meetings with clients, consultants, health plans, and internal leaders. • Shape the vision for external-facing clinical quality work and build trusted relationships. • Ensure the development of systems to monitor member journeys and maintain service reliability over time. • Utilize AI-driven quality surveillance to modernize quality operations.

Role Description La cura dell’obesità e della salute metabolica non può ridursi a una semplice prescrizione. Richiede tempo, empatia e, soprattutto, un reale lavoro di squadra. In Corposostenibile stiamo ridefinendo l'approccio al benessere e alla gestione del peso attraverso la telemedicina. Siamo una realtà innovativa nel settore della digital health, società capogruppo proprietaria di un poliambulatorio medico specialistico a Milano. Sviluppiamo percorsi scientifici avanzati basati su un modello clinico integrato, in cui medici, nutrizionisti, psicologi e coach lavorano in costante sinergia per offrire ai pazienti un percorso personalizzato e realmente sostenibile. Per ampliare il nostro team medico online, siamo alla ricerca di 2 Medici Specialisti in Endocrinologia, Scienza dell'Alimentazione o Medicina Interna che siano qualificati ed esperti nella cura dell'obesità e del sovrappeso. Qualifications - Specializzazione in Endocrinologia, Scienza dell'Alimentazione, Medicina Interna o equipollenti. - Profilo esperto nella gestione clinica del paziente con obesità/sovrappeso. - Spiccata empatia e ottime capacità di comunicazione (videochiamata e chat). - Etica professionale assoluta: rigore deontologico e appropriatezza prescrittiva (non lavoriamo con scorciatoie). Requirements - Valutazioni cliniche online e monitoraggio delle terapie farmacologiche per il dimagrimento (nel pieno rispetto delle linee guida AIFA). - Supporto clinico via chat ai pazienti all’interno del tuo turno per garantire aderenza terapeutica. - Confronto multidisciplinare costante con il resto del team (nutrizionisti, psicologi, coach). Benefits - 100% da remoto: Lavori ovunque tu sia, gestendo le visite in telemedicina. - Flessibilità oraria: Impegno di 6 ore al giorno, 5 giorni a settimana (orari da concordare, con presenza fissa in chat nelle fasce operative). - Focus totale sulla clinica: Zero burocrazia inutile e zero solitudine professionale. Al flusso amministrativo e gestionale ci pensiamo noi (con supporto software Factorial). Tu pensi solo ai pazienti. - Trattamento economico di sicuro interesse: Compenso a Partita IVA commisurato all'esperienza e alla disponibilità, capace di garantire stabilità. - Formazione inclusiva: Onboarding completo sul protocollo Corposostenibile prima della partenza. How to Apply Se vuoi far crescere un progetto sanitario innovativo e digitale, invia il tuo CV, l'attestazione di iscrizione all'Albo e una breve nota sulla tua esperienza.

Title: Medical Writing III remote type Hybrid locations Remote-United States time type Full time job requisition id R01125863 Job Description: At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue. We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you. The Impact you will make in this role: Principle Responsibilities: (essential job duties and responsibilities) - Utilizes scientific and clinical expertise, along with advanced writing and analytical skills, to research, develop, edit, format, and proofread medical and scientific publications in English. - Produces a variety of medical/scientific documents—including abstracts, posters, and manuscripts—in compliance with relevant journal and conference requirements. - Reports to the Medical Information and Publications Manager and may provide training or supervision to junior writers or contractors as needed. - Participates or leads publication panel planning meetings, contributing expertise and insights. - Works independently or collaboratively as part of a project team to accomplish assigned writing projects. - Demonstrates initiative in identifying and resolving challenges throughout the publication process. - Maintains comprehensive understanding of all Solventum product literature. - Effectively manages and prioritizes multiple projects to ensure timely completion of tasks. - Assists with special writing projects as assigned. Your Skills and Expertise To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications: - Bachelor’s degree, with 7–10 years of experience in medical and scientific publications research and authorship. - Proficient in Microsoft Office applications, including Word, Excel, Access, and PowerPoint, or equivalent PC programs. - Experience in the design, development, and authorship of publication panels. - Demonstrated expertise in medical and scientific writing principles and practices. Additional qualifications that could help you succeed even further in this role include: - Master’s or PhD degree in Science or related field - Knowledge of Solventum products - Advanced writing, critical thinking, and analytical abilities. - Exceptional communication and presentation skills. - Strong organizational skills and attention to detail, with the ability to work independently and collaboratively within a team environment. - Proven ability to interact effectively with employees and external business partners while maintaining a positive, service-oriented approach. - Demonstrated capacity to handle confidential information with discretion and exercise sound business judgment. Work location: Remote Travel: May include some [domestic/international] travel Relocation Assistance: May be authorized Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status). Supporting Your Well-being Solventum offers many programs to help you live your best life – both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope. Applicable to US Applicants Only:The expected compensation range for this position is $137,439 - $167,981, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status. Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly. Solventum Global Terms of Use and Privacy Statement Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at Solventum are conditioned on your acceptance and compliance with these terms.