Únete a Thermo Fisher ScientificHaz un impacto global a través de un trabajo significativo todos los días, contribuyendo a soluciones para desafíos como la protección ambiental y tratamientos contra el cáncer.Información del Localización y DivisiónBogotá, Colombia / División de ensayos clínicos.¿Cómo Harás un Impacto?Gestionarás proyectos logísticos desde el inicio hasta la conclusión del estudio.Un Día en la VidaComo Gerente de Proyectos de Servicios al Cliente II, serás responsable de:Coordinar los cronogramas de proyectos y asegurar la implementación exitosa de los requisitos del cliente.Colaborar diariamente con equipos multifuncionales para brindar un servicio al cliente de clase mundial.Identificar riesgos del proyecto y desarrollar estrategias para mitigarlos.Monitorear y adherirse estrictamente a los estándares de calidad para ofrecer resultados impecables.Requisitos de EducaciónDiploma de secundaria o experiencia equivalente en administración, logística o ingeniería requerida.ExperienciaMínimo 2 años de experiencia laboral en logística, gestión de proyectos o un campo relacionado.Historial comprobado en servicio al cliente y gestión de proyectos preferido.Conocimientos, Habilidades y CapacidadesFuertes habilidades organizativas y de multitarea.Excelentes habilidades de comunicación e interpersonales.Dominio en software y herramientas de gestión de proyectos.Capacidad para trabajar de manera colaborativa en un entorno orientado al equipo.Requisitos Físicos / Ambiente de TrabajoPuesto basado en oficina con viajes ocasionales a sitios de clientes.Capacidad para trabajar en un ambiente de ritmo acelerado y priorizar tareas de manera efectiva.Lo Que OfrecemosCompensaciónSalario competitivo y paquete de beneficios.Bonificación y aumento basado en el desempeño anual.Excelentes BeneficiosBeneficios médicos, dentales y de visión desde el primer día.Tiempo libre pagado y días festivos designados.Plan de ahorro para jubilación con contribución del empleador.Reembolso de matrícula para aprendizaje continuo.Bonificación por referencia de empleados.Oportunidades de avance profesional dentro de un líder global en servicios científicos.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office, Warehouse Join Thermo Fisher Scientific to make a global impact through meaningful work every day. Help develop solutions for tough challenges like environmental protection and cancer cures. Location/Division Specific Information: (Bogotá, Colombia / Clinical trials division) How Will You Make an Impact?: Provide management of logistics projects from the beginning (start-up), during, and until the completion of the study. A Day in the Life: As a Client Services Project Manager II, you will: Coordinate project timelines and ensure successful implementation of client requirements.Collaborate daily with cross-functional teams to deliver world-class customer service.Determine project risks and develop strategies to mitigate them.Monitor and strictly adhere to quality standards to deliver flawless results. Education: High school diploma or equivalent experience in administration, logistics, or engineering required. Experience: Minimum of 2 years of work experience in logistics, project management, or a related field required.Proven track record in customer service and project management preferred. Knowledge, Skills, Abilities: Strong organizational and multitasking skills.Excellent communication and interpersonal abilities.Proficiency in project management software and tools.Ability to work collaboratively in a team-oriented environment. Physical Requirements / Work Environment: Office-based role with occasional travel to client sites.Must be able to work in a fast-paced environment and prioritize tasks effectively. What We Offer Compensation Competitive salary and benefits package.Annual performance-based bonus and merit increase. Excellent Benefits Medical, Dental, & Vision benefits-effective Day 1.Paid Time Off & Designated Paid Holidays.Retirement Savings Plan with employer match.Tuition Reimbursement for continuous learning.Employee Referral Bonus.Career Advancement Opportunities within a global leader in scientific services.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Thermo Fisher Scientific offers impactful work globally, enabling customers to improve health and safety. We have a vacancy for a Senior ICF Medical Writing Project Manager based in Mexico. Discover Impactful Work: Lead ambitious initiatives that craft the future of clinical research. Your expertise will enable us to deliver flawless Informed Consent Forms (ICFs) and other critical documents, ensuring outstanding quality and compliance. A day in the Life: Develop project timelines, standards, budgets, and forecasts.Collaborate with cross-functional teams to meet deliverables.Monitor timelines and provide status updates.Identify and resolve client management issues.Ensure compliance with quality processes. Keys to Success: Proven project management skills.Strong planning and organizational abilities.Excellent interpersonal and communication skills.Ability to work independently and under pressure. Education Prefer BS/BA in a scientific field with 5 years experience, or an advanced degree with 3 years experience. Experience Experience managing medical writing or clinical projects.Pharmaceutical/CRO industry experience preferred.Advantageous to have experience in regulatory and/or plain language medical writing. Knowledge, Skills, Abilities Solid project management, budgeting, and forecasting skills.Effective problem-solving and decision-making abilities.Proficient in global and regional regulatory guidelines. Physical Requirements / Work Environment Office-based role with exposure to electrical office equipment.Occasional travel to client sites; domestic and rare international travel.Frequent stationary periods, hand movements, and light lifting (15-20 lbs). Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Responsible for Sales representative for Chile region, with the goal of growing the business and achieving Sales Targets. Work together with Local Manager to develop account and territory planning to sell products and workflows of LSG. Study and have a good technical understanding of Biology and Genetics Sciences products to promote technical and consultative sales. Supervise and analyze sales results, develop new customers, promote and introduce new products through daily customer visits. Build an accurate forecast and be accountable for the numbers. Meet territory targets. Participate in Congresses, Seminars and Workshops. Understand and build strategical plans to beat competition in the territory. Complaint with ThermoFisher rules. Main Activities: Identify, visit and follow up all of the potential customers. Main objective is to over achieve AOP.Develop opportunities for Biology and genetics sciencesLearn and adopt an standardized process for: 1. Funnel management – deep understanding, assignation of opportunities, dispute resolution and 2. Forecasting for all leads in the territory – advance AOP achievement, raise/bring up issues and ask for help.Detect and document plans regarding customer´s investment opportunities such as: quote, offer , marketing and sales tools support, organize technical presentations or demonstrations of our products. Responsible for providing proper support to pre and post sales activities.Serve as the Single Point of Contact for customers in the Chile region regarding: support, information and any other related requestsDrive and ensure full ethics and compliance as well as regulatory practices according to company standards.Develop new customer, introduce new products and workflows in existing customersAttend technical trainingsBuild funnel pipeline and join forecast calls – analyze sales results and market trendsDevelop territory and account planningHit sales targetsPromote ThermoFisher brands Competencies: Customer experience focusStrong business insightTeam playerAbility to understand and apply market knowledge into Sales StrategyAbility to influence customersCommercial/ Forecast accuracy skills Minimum requirements: Biological graduation (Biology, Pharmacy, Biomedical, etc), preferably with Master and/or PhD in the same area50% English Fluence (writing and speaking)30 -50% travel availability2-3 years commercial experience

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Actividades principales: COTIZACIONES (30 minutos por cotización)Revisar con fábrica disponibilidad del repuesto y precio de venta si el código consultado no está en Lista de PreciosGenerar cotización, Registrar en Control xx para llevar orden y enviar CotizaciónSi está descontinuado, informar al cliente respectivo reemplazo y nuevo precio.Pedir a fábrica datasheet por el código reemplazado.Segumiento Cotizaciones. El tiempo puede variar cuando se trata de Spares que no se encuentran en lista de precios donde podría demorar 48 a 72 horas REVISIÓN DE PORTALES (30 minutos)PROCESAMIENTO DE UNA ORDEN (30 minutos)Revisión de orden de compra recibidaRevisión OC portal / Confirmar / Descargar OCConfirmación datos OC vs Control MineralsCreación de Nota de ventaCreación de IC PO y envío a COMEX: Revisión de precios IC, Precios venta, Lead TimeResponder al cliente su orden en procesoRegistrar nueva orden en Reporte Backlog semanalRegistro de pedido en planilla de Control Confirmación recepción de órdenes de compra y actualización de fechas hacia el cliente REVISIÓN CONFIRMACIÓN DE FÁBRICA Y LLENADO DE PLANILLA DE CONTROL (45 a 60 minutos)Revisión y registro en Control Minerals, Registro de códigos, cantidad, precio compra, fecha de entrega.Informar al cliente fecha estimada de entrega.En caso de error en IC, corregir.Si fábrica informa obsolesencia de Item y respectivo reemplazo, se informa al cliente.Cotizar nuevo código, pedir actualizar orden de compra. Enviar algún datasheet que consigamos de fábrica para respaldar el cambio.ENTREGA DE ORDEN DE COMPRA EN FÁBRICA (60 minutos)CS revisa documentación de fábrica para que no haya diferencias entre lo que se entrega y lo solicitado por el cliente.Seguimiento al cliente para que recolecteCliente recolecta cargaCS revisa factura fábrica, shipping documentsCS solicita a Finanzas emitir factura adjuntando: OC cliente, factura fábrica, respaldos de recolección, informa detalle a factura. Orden parcial o completa de respectiva Nota de Venta

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Responsible for Sales representative for Chile region, with the goal of growing the business and achieving Sales Targets. Work together with Local Manager to develop account and territory planning to sell products and workflows of LSG. Study and have a good technical understanding of Biology and Genetics Sciences products to promote technical and consultative sales. Supervise and analyze sales results, develop new customers, promote and introduce new products through daily customer visits. Build an accurate forecast and be accountable for the numbers. Meet territory targets. Participate in Congresses, Seminars and Workshops. Understand and build strategical plans to beat competition in the territory. Complaint with ThermoFisher rules. Main Activities: Identify, visit and follow up all of the potential customers. Main objective is to over achieve AOP.Develop opportunities for Biology and genetics sciencesLearn and adopt an standardized process for: 1. Funnel management – deep understanding, assignation of opportunities, dispute resolution and 2. Forecasting for all leads in the territory – advance AOP achievement, raise/bring up issues and ask for help.Detect and document plans regarding customer´s investment opportunities such as: quote, offer , marketing and sales tools support, organize technical presentations or demonstrations of our products. Responsible for providing proper support to pre and post sales activities.Serve as the Single Point of Contact for customers in the Chile region regarding: support, information and any other related requestsDrive and ensure full ethics and compliance as well as regulatory practices according to company standards.Develop new customer, introduce new products and workflows in existing customersAttend technical trainingsBuild funnel pipeline and join forecast calls – analyze sales results and market trendsDevelop territory and account planningHit sales targetsPromote ThermoFisher brands Competencies: Customer experience focusStrong business insightTeam playerAbility to understand and apply market knowledge into Sales StrategyAbility to influence customersCommercial/ Forecast accuracy skills Minimum requirements: Biological graduation (Biology, Pharmacy, Biomedical, etc), preferably with Master and/or PhD in the same area50% English Fluence (writing and speaking)30 -50% travel availability2-3 years commercial experience

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Are you an ambitious and proven professional looking for an exceptional opportunity to showcase your strong work ethic and skills? Thermo Fisher Scientific Inc. is seeking an individual with a track record of success in Vendor Management to join our world-class team of researchers. As a leader in the scientific industry, we are dedicated to enabling our customers to make the world healthier, cleaner, and safer. Responsibilities: Collaborate with cross-functional teams to determine vendor requirements and establish sourcing strategies Manage vendor relationships and contracts, ensuring flawless execution and delivery Conduct market research and competitive analysis to identify potential vendors Develop and implement vendor performance metrics and conduct regular evaluations Drive continuous improvement initiatives to optimize vendor management processes Requirements: Bachelor's degree in Business Administration or related field, or equivalent experience in the industry. Previous experience in vendor management or procurement Strong analytical and negotiation skills Excellent communication and interpersonal skills Proven ability to successfully implement vendor management strategies At Thermo Fisher Scientific, we value diversity and inclusivity. We believe that collaboration and different perspectives drive innovation and lead to exceptional results. We are an equal opportunity employer and strictly prohibit discrimination based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. If you require any accommodations during the application process due to a disability, we are here to support you. Please contact us at 1-855-471-2255* to request assistance. Our commitment to accessibility ensures that all qualified individuals have an equal opportunity to compete for our positions. Apply today and start your journey with Thermo Fisher Scientific Inc. to contribute to groundbreaking research and make a difference in the world. Visit our website at http://jobs.thermofisher.com to apply now.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office The North American Regulatory Affairs Lead (RAL) provides innovative regulatory solutions and expertise to support product development from preclinical stages through registration and product optimization. This role involves strategic intelligence and guidance, ensuring that client deliverables meet current local, regional, and ICH regulatory and technical requirements. The RAL acts as a liaison with internal and external clients and oversees the preparation and submission of regulatory documentation. Essential Functions: Support the preparation of documentation and submissions under guidance.Coordinate and manage client deliverables ensuring regulatory compliance.Liaise with internal and external clients to track and update the status of long-range planning, adapting to changing priorities and handling multiple projects.Exhibit good negotiation skills and the capability to work independently with direction, exercising independent judgment.Independently assess sponsor regulatory needs and collaborate with project team members to produce compliant deliverables.Possess basic knowledge of global/regional/national country requirements and regulatory affairs procedures for clinical trial authorization, licensing, and lifecycle management.Understand medical terminology, statistical concepts, and guidelines.Demonstrate good analytical, investigative, and problem-solving skills, with the ability to interpret data. New Tasks and Responsibilities: Accountable and responsible for overseeing all submission types to Regulatory Authorities and/or EC/other local submissions, including North America IRB submissions.Manage country-specific local applications, overseeing the entire process from preparation to approval.Collect regulatory requirements and coordinate country-specific local applications, relying on RegView entries and follow-ups with CASs.Ensure adherence to standard RAL procedures applicable to EC and RA submissions.Oversee the development, translation, and filing of country and site-specific submission-related documents for RA, US IRBs and Canadian ECs submissionsEnsure that submission-related documents are received within the agreed timeline and filed according to agreed processes.Inform all Lead RAL and/or functional leads of the required deadlines for submission document availability.Liaise with Lead RAL and/or responsible functional leads in the CRG internal team to ensure documents required for submission are ready in time as per the submission plan. Working Conditions and Environment: Work is performed in an office environment with exposure to electrical office equipment.Occasional drives to site locations with occasional travel, both domestic and international. Physical Requirements: Coordinate all North America IRB activities and ensure that essential document quality meets the expectations of Regulatory Compliance Review.Ensure timely North America regulatory and/or IRB submissions and follow up on all questions raised by ethics committees. Management Role: No management responsibility. This role requires a highly organized individual with strong regulatory expertise and the ability to manage multiple projects and adapt to changing priorities. The successful candidate will possess excellent communication and negotiation skills, along with a basic understanding of the regulatory landscape and procedures. Qualifications: Education and Experience: Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years) Knowledge, Skills and Abilities: Good English language (written and oral) communication skills as well as local language where applicableGood attention to detail and quality as well as editorial/proofreading skillsGood interpersonal skills to work effectively in a team environmentGood computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologiesBasic organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projectsGood negotiation skillsCapable of working independently with direction and exercising independent judgmentCapable of independently assessing sponsor regulatory needs and working with project team members in producing compliant deliverablesBasic knowledge of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization, licensing, lifecycle managementBasic understanding of medical terminology, statistical concepts, and guidelinesGood analytical, investigative and problem-solving skills Capable of interpreting data

Work Schedule Standard (Mon-Fri) Environmental Conditions Office OBJETIVOS GENERALES DEL PUESTO: Identificar, confeccionar y presentar ofertas comerciales para venta con el sector público. Analizar bases y condiciones de las contrataciones públicas en sus distintas modalidades (Licitaciones, Compras Agiles, Tratos Directos, Cotizaciones y Consultas al Mercado). Analizar documentos y marco regulatorio relacionado a las oportunidades comerciales, siguiendo la normativa corporativa, las nomas del compliance y el marco legal vigente del país. RESPONSABILIDADES DEL PUESTO: Captura de ofertas e identificación de oportunidades a través de distintos canales (Falcon Soft – Portal mercado Publico) y enviarlos al equipo comercial.Realizar consultas y aclaraciones en el foro del Portal MP cuando algún proceso de compra lo requiera.Administrar y controlar la documentación necesaria al momento de presentar una oferta.Preparar ofertas para ser presentada en el Portal Mercado Publico.Velar que los procesos de venta pública se ejecuten siguiendo la política interna de acuerdo con la normativa aplicable.Análisis detallado de cada oportunidad (condiciones y requisitos de las bases y sus distintos anexos)Remitir cuando sea requerido, declaraciones a los organismos públicos, ejemplo: declaraciones juradas, notas, aclaraciones, garantías (pólizas).Solicitar garantías de seriedad, fiel cumplimiento de contrato y anticipo.Registro y control de las oportunidades con los datos de cada proceso: Datos de la Oferta, Comparativas de Precios, Órdenes de Compra etc.Trabajo continuo con el equipo comercial y áreas operativas (Servicio al cliente, Finanzas, Logística, Legales).Revisión y control del proceso licitatorio, desde la identificación de la oportunidad hasta la entrega de lo adjudicado.Análisis y control de multas cuando estas sean notificadas. Analizar el proceso para la realización de descargos y/o confirmar el pago de la multa cuando corresponda.Recepcion de las Órdenes de Compra, controlar lo adjudicado y enviar a procesar pedido de entrega con las áreas funcionales de la empresa (Servicio al cliente)Seguimiento de los pedidos en coordinación con las áreas operativas, detectando inconsistencias y generando acciones para mitigar entregas retrasadas.Elaborar informes para la Gerencia. COMPETENCIAS TÉCNICA: Experiencia preparando oportunidades de negocio con el sector público (Licitaciones, Compras Agiles, Tratos Directos, Cotizaciones y Consultas al Mercado).Experiencia en industria Biotech, Farmacéutica, dispositivos médicos, etc.Conocimiento de la herramienta Falcon Soft en los Módulos de Búsqueda, Gestión y Análisis. (Deseable)Manejo de la suite Office 365 – Teams – One Drive – SharepointDominio de Excel Intermedio – Avanzando comprobable (Tablas dinámicas, buscar v, formulas condicionales)Ingles Intermedio (principalmente lectura y escritura)Experiencia usando algún CRM (Sap – JD Edwards – Sales Force) APTITUDES OrganizaciónLiderazgoSentido de urgenciaSeguimiento y discreciónProactividadComunicaciónTrabajo en equipoCompromisoDiscreción y manejo de información sensibleFoco en el cliente y en el resultado CALIFICACIÓN MÍNIMA Escolaridad mínima secundario completo y/o estudiante de Administración, Economía, Contaduría, AbogacíaCursos Paquete Office Intermedio, Sistemas SAPTiempo de Experiencia 4 años en Licitaciones y ventas al sector público dentro de la industria del cuidado de la salud

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Are you an ambitious and proven professional looking for an exceptional opportunity to showcase your strong work ethic and skills? Thermo Fisher Scientific Inc. is seeking an individual with a track record of success in Vendor Management to join our world-class team of researchers. As a leader in the scientific industry, we are dedicated to enabling our customers to make the world healthier, cleaner, and safer. Responsibilities: Collaborate with cross-functional teams to determine vendor requirements and establish sourcing strategies Manage vendor relationships and contracts, ensuring flawless execution and delivery Conduct market research and competitive analysis to identify potential vendors Develop and implement vendor performance metrics and conduct regular evaluations Drive continuous improvement initiatives to optimize vendor management processes Requirements: Bachelor's degree in Business Administration or related field, or equivalent experience in the industry. Previous experience in vendor management or procurement Strong analytical and negotiation skills Excellent communication and interpersonal skills Proven ability to successfully implement vendor management strategies At Thermo Fisher Scientific, we value diversity and inclusivity. We believe that collaboration and different perspectives drive innovation and lead to exceptional results. We are an equal opportunity employer and strictly prohibit discrimination based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. If you require any accommodations during the application process due to a disability, we are here to support you. Please contact us at 1-855-471-2255* to request assistance. Our commitment to accessibility ensures that all qualified individuals have an equal opportunity to compete for our positions. Apply today and start your journey with Thermo Fisher Scientific Inc. to contribute to groundbreaking research and make a difference in the world. Visit our website at http://jobs.thermofisher.com to apply now.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office The North American Regulatory Affairs Lead (RAL) provides innovative regulatory solutions and expertise to support product development from preclinical stages through registration and product optimization. This role involves strategic intelligence and guidance, ensuring that client deliverables meet current local, regional, and ICH regulatory and technical requirements. The RAL acts as a liaison with internal and external clients and oversees the preparation and submission of regulatory documentation. Essential Functions: Support the preparation of documentation and submissions under guidance.Coordinate and manage client deliverables ensuring regulatory compliance.Liaise with internal and external clients to track and update the status of long-range planning, adapting to changing priorities and handling multiple projects.Exhibit good negotiation skills and the capability to work independently with direction, exercising independent judgment.Independently assess sponsor regulatory needs and collaborate with project team members to produce compliant deliverables.Possess basic knowledge of global/regional/national country requirements and regulatory affairs procedures for clinical trial authorization, licensing, and lifecycle management.Understand medical terminology, statistical concepts, and guidelines.Demonstrate good analytical, investigative, and problem-solving skills, with the ability to interpret data. New Tasks and Responsibilities: Accountable and responsible for overseeing all submission types to Regulatory Authorities and/or EC/other local submissions, including North America IRB submissions.Manage country-specific local applications, overseeing the entire process from preparation to approval.Collect regulatory requirements and coordinate country-specific local applications, relying on RegView entries and follow-ups with CASs.Ensure adherence to standard RAL procedures applicable to EC and RA submissions.Oversee the development, translation, and filing of country and site-specific submission-related documents for RA, US IRBs and Canadian ECs submissionsEnsure that submission-related documents are received within the agreed timeline and filed according to agreed processes.Inform all Lead RAL and/or functional leads of the required deadlines for submission document availability.Liaise with Lead RAL and/or responsible functional leads in the CRG internal team to ensure documents required for submission are ready in time as per the submission plan. Working Conditions and Environment: Work is performed in an office environment with exposure to electrical office equipment.Occasional drives to site locations with occasional travel, both domestic and international. Physical Requirements: Coordinate all North America IRB activities and ensure that essential document quality meets the expectations of Regulatory Compliance Review.Ensure timely North America regulatory and/or IRB submissions and follow up on all questions raised by ethics committees. Management Role: No management responsibility. This role requires a highly organized individual with strong regulatory expertise and the ability to manage multiple projects and adapt to changing priorities. The successful candidate will possess excellent communication and negotiation skills, along with a basic understanding of the regulatory landscape and procedures. Qualifications: Education and Experience: Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years) Knowledge, Skills and Abilities: Good English language (written and oral) communication skills as well as local language where applicableGood attention to detail and quality as well as editorial/proofreading skillsGood interpersonal skills to work effectively in a team environmentGood computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologiesBasic organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projectsGood negotiation skillsCapable of working independently with direction and exercising independent judgmentCapable of independently assessing sponsor regulatory needs and working with project team members in producing compliant deliverablesBasic knowledge of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization, licensing, lifecycle managementBasic understanding of medical terminology, statistical concepts, and guidelinesGood analytical, investigative and problem-solving skills Capable of interpreting data

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Thermo Fisher Scientific offers impactful work globally, enabling customers to improve health and safety. We have a vacancy for a Senior ICF Medical Writing Project Manager based in Mexico. Discover Impactful Work: Lead ambitious initiatives that craft the future of clinical research. Your expertise will enable us to deliver flawless Informed Consent Forms (ICFs) and other critical documents, ensuring outstanding quality and compliance. A day in the Life: Develop project timelines, standards, budgets, and forecasts.Collaborate with cross-functional teams to meet deliverables.Monitor timelines and provide status updates.Identify and resolve client management issues.Ensure compliance with quality processes. Keys to Success: Proven project management skills.Strong planning and organizational abilities.Excellent interpersonal and communication skills.Ability to work independently and under pressure. Education Prefer BS/BA in a scientific field with 5 years experience, or an advanced degree with 3 years experience. Experience Experience managing medical writing or clinical projects.Pharmaceutical/CRO industry experience preferred.Advantageous to have experience in regulatory and/or plain language medical writing. Knowledge, Skills, Abilities Solid project management, budgeting, and forecasting skills.Effective problem-solving and decision-making abilities.Proficient in global and regional regulatory guidelines. Physical Requirements / Work Environment Office-based role with exposure to electrical office equipment.Occasional travel to client sites; domestic and rare international travel.Frequent stationary periods, hand movements, and light lifting (15-20 lbs). Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Thermo Fisher Scientific offers impactful work globally, enabling customers to improve health and safety. We have a vacancy for a Senior ICF Medical Writing Project Manager based in Mexico. Discover Impactful Work: Lead ambitious initiatives that craft the future of clinical research. Your expertise will enable us to deliver flawless Informed Consent Forms (ICFs) and other critical documents, ensuring outstanding quality and compliance. A day in the Life: Develop project timelines, standards, budgets, and forecasts.Collaborate with cross-functional teams to meet deliverables.Monitor timelines and provide status updates.Identify and resolve client management issues.Ensure compliance with quality processes. Keys to Success: Proven project management skills.Strong planning and organizational abilities.Excellent interpersonal and communication skills.Ability to work independently and under pressure. Education Prefer BS/BA in a scientific field with 5 years experience, or an advanced degree with 3 years experience. Experience Experience managing medical writing or clinical projects.Pharmaceutical/CRO industry experience preferred.Advantageous to have experience in regulatory and/or plain language medical writing. Knowledge, Skills, Abilities Solid project management, budgeting, and forecasting skills.Effective problem-solving and decision-making abilities.Proficient in global and regional regulatory guidelines. Physical Requirements / Work Environment Office-based role with exposure to electrical office equipment.Occasional travel to client sites; domestic and rare international travel.Frequent stationary periods, hand movements, and light lifting (15-20 lbs). Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Work Schedule Environmental Conditions Summarized Purpose: Provides complete oversight of supply chain for sophisticated global clinical trials. Ensures project/study activities are in compliance with company and client requirements. Acts as a representative for the department on all assigned projects. Develops study specific plans for each assigned project.  Meets with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/spreadsheets.  Integrates all clinical supplies activities into the supply chain to support project logistic strategy and compliance with GxP requirements.  Participates in ongoing training on new regulations.  Represents the department internally and externally at meetings, strategic projects and initiatives as per the business requirements.  Mentors and guides supports junior team members.  Participates in process improvement initiatives.  Maintains and uses existing tools while continously looking for improvement opportunities.  May participate in the bidding and/or bid defense opportunities  client contact for their supply chain requests/questions/concerns Education and Experience: Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).