Amgen bogota, d.c., capital district, colombia join or sign in to find your next job join to apply for the commercial pricing manager (bogotá) role at amgen amgen bogota, d.c., capital district, colombia 2 days ago be among the first 25 applicants join to apply for the commercial pricing manager (bogotá) role at amgen get ai-powered advice on this job and more exclusive features. join amgen’s mission of serving patients at amgen, if you feel like you’re part of something bigger, it’s because you are. our shared mission—to serve patients living with serious illnesses—drives all that we do. since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. with our focus on four therapeutic areas –oncology, inflammation, general medicine, and rare disease– we reach millions of patients each year. as a member of the amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. our award-winning culture is collaborative, innovative, and science based. if you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the amgen team. join us and transform the lives of patients while transforming your career. commercial pricing manager ( bogotá) what you will do let’s do this. let’s change the world. in this vital role you will a strategic and results-driven pricing manager to join our team in colombia, focusing on the pharmaceutical and biotechnology sectors....
Join to apply for the medical science liaison sr - oncología role at servier andean, central america & caribbean. get ai-powered advice on this job and more exclusive features. descripción del puesto misión enlace médico-científico para oncología. responsable del diseño e implementación de la estrategia médica en su región, de acuerdo con la estrategia médica de la filial y en coordinación con otros departamentos, con el fin de desarrollar el valor médico, el desarrollo y el acceso a las soluciones terapéuticas de servier en beneficio de los pacientes. proporcionar soporte científico y médico en campo en las zonas asignadas. responsabilidades colaboración y representación de los intereses de servier ancac en interacciones con expertos en áreas terapéuticas (taes), sociedades médicas y centros de referencia en las zonas bajo su responsabilidad, mediante actividades educativas y análisis de evidencia clínica. definir, establecer, ejecutar y hacer seguimiento a los planes de acción médicos regionales, incluyendo reuniones hospitalarias, mesas redondas, optimización de gestión del paciente y protocolos de investigación. gestionar la comunicación científica de datos clínicos, de desarrollo o publicaciones, manteniendo contacto actualizado y presentando materiales científicos. colaborar con otros departamentos, promoviendo actividades educativas y comunicando información científica relevante a actores internos. seguir los estándares de compliance, políticas internas y legislaciones vigentes en todas sus actividades. región de operación: colombia. requisitos profesional en medicin...
Principal biostatistician | clinical | pharma (fsp) top global pharma (fsp) via global cro fully remote fte who will you be working with? you'll be dedicated to a global pharmaceutical powerhouse driven by science, powered by data, and inspired by a deep commitment to reimagining medicine. their pipeline is among the most robust in the industry, fueled by cutting-edge research, strategic partnerships, and a bold embrace of emerging technologies like gene therapy, ai, and digital health. operating across more than 100 countries, they blend global impact with a mission rooted in improving and extending lives. what will you be doing? lead statistical analysis plans and oversee saps, protocols, and reporting act as a global lead across multiple studies and regulatory interactions produce and validate complex efficacy outputs and randomisation schemes mentor junior statisticians, with potential for line management work closely with clinical scientists and cross-functional teams what can you bring to the table? m.s. or ph.d. degree in statistics, biostatistics, or related field. experience in statistics, biostatistics or related field proven experience must be in a cro or pharmaceutical environment what to do next… apply directly or share a copy of your resume to #j-18808-ljbffr...
Iqvia bogota, d.c., capital district, colombia join or sign in to find your next job join to apply for the visitador médico virtual role at iqvia iqvia bogota, d.c., capital district, colombia join to apply for the visitador médico virtual role at iqvia get ai-powered advice on this job and more exclusive features. actualmente nos encontramos en la búsqueda de profesionales de áreas de la salud y/o administrativas, que quieran ser parte de un gran proyecto con una importante compañía farmacéutica visitador médico virtual objetivo del cargo responsable de la educación y promoción del portafolio de salud dirigido a médicos de diferentes especialidades a través de una plataforma web y telefónica; garantizando el cumplimiento del presupuesto de venta asignado, el crecimiento de su zona y el seguimiento al ciclo promocional de los productos. principales funciones promocionar portafolio al panel asignado a su territorio a través de diferentes plataformas virtuales y de manera presencial. construir relaciones efectivas con su panel asignado. asegurar las metas de venta establecidas para su territorio. mantener actualizada toda la información de su panel. manejar de herramientas para la gestión de su territorio. conocer el portafolio que promociona. adherirse a los lineamientos de ética en los negocios. requisitos profesionales de áreas de la salud y/o administrativas. experiencia de 1 año en adelante en posiciones similares, preferiblemente manejando líneas de consumo masivo o primary care. manejo de paquete office y herramientas de marketing...
This position is responsible for project management and study site management from site selection toinitiation until monitoring and close-out of assigned clinical study studies in accordance with tigermedor sponsor standard operating procedures (sops), international conference on harmonization goodclinical practice standard (ich-gcp), clinical practice standard (gcp) and other applicableregulations; the position is responsible for ensuring that all data generated by the assigned sites is of high quality,on time and within budget. 2. responsibilities: study site selection, initiation (siv) and clinical monitoring; provide ongoing training to site staff with regards to ich-gcp, gcp, study protocol and requirements; conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements; ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. maintain and update these documents in investigator files, trial master files; prepare/complete study records’ archiving according to protocol and sponsor requirements; ensure safety information is disseminated to all sites according sop and applicable regulations; ensure sae is reported within the timeline in compliance with sops and applicable regulations; finalize budget and obtain signed contract from site, prior to site initiation visit; ensure study payment schedule is executed and retain relevant documents/receipts; update and maintain study tools/systems in a timely manner. 3. qualifications: bachelor ...
Join to apply for the logistics specialist i role at thermo fisher scientific join to apply for the logistics specialist i role at thermo fisher scientific work schedule standard (mon-fri) environmental conditions office logistics specialist i join thermo fisher scientific inc. and excel in an exceptionally dynamic role as a logistics specialist i in bogota. this position offers a fantastic opportunity to collaborate with a world-class team and successfully implement logistics operations critical to advancing clinical projects. responsibilities coordinate product receipts from the arrival at our facilities until release in the gpm system. process medication and supply orders to medical facilities and request receipt acknowledgments. collaborate on new project initiations and coordinate with medical centers for shipment and return of materials. generate administrative starts for projects, crafting necessary folders and forms. monitor material transfer processes and request final product disposals. advise medical centers on shipment procedures, storage conditions, and documentation. detect and report deviations, complete investigations, and propose process improvements. collaborate in reception, dispatch, and return processes, ensuring deadlines are met. perform monthly service registrations, attend to comments, and ensure timely registration. develop metrics for suppliers, performance indicators, and reports for customers. complete all activities efficiently and safely. requirements bachelor's degree in engineering, logistics operatio...
Join to apply for the supervisor(a) validacion metodos analiticos role at vaxthera . join our team as an analytical methods validation supervisor, where you will lead the development and implementation of strategies and policies related to analytical methods validation in our quality control department. with a strong foundation in analytical chemistry, microbiology, and vaccine development, you'll ensure compliance with regulatory guidelines (ich, who, fda, ema) and pharmacopeias (usp, bp) while working closely with the quality control team to overcome challenges in commercial testing. your expertise will guide inspections and audits as you uphold data integrity within validation functions. responsibilities developing and implementing validation strategies for analytical methods. designing, executing, and documenting validation studies for vaccines. coordinating analytical method transfers with the quality control team. ensuring compliance with sops and regulatory requirements. reviewing and approving sops, protocols, and validation reports. managing qms compliance regarding change controls, deviations, etc. handling inspections and audits as an expert in method validation. requirements professional degree in sciences (life sciences), engineering, chemistry, pharmaceutical chemistry, biochemistry, or microbiology. minimum 3 years of experience in analytical method validation. strong foundation in analytical chemistry, microbiology, and vaccines. practical experience in biochemical and immunological methods for vaccines. education level professional hard skills regulatory gu...
Iqvia bogota, d.c., capital district, colombia join or sign in to find your next job join to apply for the especialista calidad y procesos psp role at iqvia iqvia bogota, d.c., capital district, colombia join to apply for the especialista calidad y procesos psp role at iqvia get ai-powered advice on this job and more exclusive features. especialista calidad y procesos (licencia de maternidad) descripción: ¡Únete a nosotros en nuestro emocionante trayecto! iqvia es the human data science company , enfocada en el uso de datos y ciencia para ayudar a los clientes de la salud a encontrar mejores soluciones para sus pacientes. formada a partir de la fusión de ims health y quintiles, iqvia ofrece una amplia gama de soluciones que aprovechan los avances en información, tecnología, análisis e ingenio humano para impulsar la atención médica. objetivo: gestionar que nuestros procesos y áreas de negocio se rijan bajo las mejores prácticas, normas de calidad y de gestión, a fin de garantizar nuestra eficiencia y cumplimiento de la norma en cada una de las operaciones. responsabilidades: implementar y gestionar documentación que apoye en la estandarización de procesos del área de calidad de iqvia latam adaptar y reutilizar los procesos existentes en el marco del sistema de gestión integrado iso 9001 para países de latam documentar los procesos de nuestros servicios de programas de soporte a pacientes y farmacovigilancia. implementar procesos de auditorías para nuestro servicio garantizando la calidad y cumplimiento de estos, identificando posibles ...
Career category sales & marketing operations job description join amgen’s mission of serving patients at amgen, if you feel like you’re part of something bigger, it’s because you are. our shared mission—to serve patients living with serious illnesses—drives all that we do. since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. with our focus on four therapeutic areas –oncology, inflammation, general medicine, and rare disease– we reach millions of patients each year. as a member of the amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. our award-winning culture is collaborative, innovative, and science based. if you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the amgen team. join us and transform the lives of patients while transforming your career. commercial pricing manager ( bogotá) what you will do let’s do this. let’s change the world. in this vital role you will a strategic and results-driven pricing manager to join our team in colombia, focusing on the pharmaceutical and biotechnology sectors. this critical role will be responsible for designing, implementing, and monitoring pricing strategies that align with business objectives, ensure regulatory compliance, and strengthen our competitive position in the market. the pricing manager will collaborate with cross-functional teams to drive profitability and optimize pricing models for in...
As a clinical research associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies and vaccines for many of the world’s most challenging diseases including cancer, cardio-metabolic diseases, alzheimer’s and infectious diseases. be ready to work in a solid partnership and an environment driven by innovation and continuous improvement. what you will be doing: completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes. verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. participates in audit preparation and follow-up activities as needed. may serve as preceptor, providing training to less experienced clinical team members. you are: bachelor’s degree in a health, life sciences or other relevant field of study. previous experience supporting clinical trials including 4 years of experience on site monitoring tasks. pr...
Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: oncology, rare disease and neuroscience. supported by nearly 100 years of development experience, with global hubs in the u.s., france and the u.k, we tackle areas of high unmet medical need through research and innovation. our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. we build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. at ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. join us on our journey towards sustainable growth, creating real impact on patients and society! build and follow the marketing strategy to insure the product development : design brand plan and long term 5y plan. create an implement the brand strategy and product positioning. execute the brand plan’s activities. comply with the sales and investment budget. analyze the market data to find business opportunities. accompaniment in field work to the sales force develop communication and promotion campaigns. establish and maintain relationship with kols. reinforce the synergies across all sales representatives, commercial and access team. coordinate logistics to enable pre-launch products sourcing and delivery to the market in cooperation with the logistics area. provide technical expertise, training, and motivation to the field force on the products and client...
Country market access & pricing manager we are an innovative global healthcare company with a focus on immunology that extends to innovation in diabetes and transplant medicine. across different countries, our talented teams are determined to deliver a best-in-class customer experience using the best of digital, artificial intelligence and personal know-how. with a focus on immunology that extends to innovation in diabetes and transplant medicines, we pursue progress to make a real impact on millions of patients around the world. manages the timely and comprehensive access of sanofi therapies within the colombian healthcare system through the management of assigned ecosystems (insurers, providers, and pharmaceutical managers). responsible for delivering the product value proposition and other health value solutions to payers. accountable for the ongoing development, refinement and execution of local payer strategy, plans and tactics for the sanofi pharma portfolio products throughout the lifecycle. ensures alignment with local market access functions and cross-functional local teams to build and adapt successful access strategies and tools for the benefit of sanofi. is responsible for the development of the market access blueprint at the affiliate level (adapting the global market access blueprint to local needs). as a result, also accountable for sales management within the defined clients of these ecosystems. organizational context: this position will focus on sanofi pharma portfolio. the occupant will report to market access head copac. major responsibilities and activit...
Home based icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. we are currently seeking a pharmacovigilance associate to join our diverse and dynamic team. as a pharmacovigilance associate at icon, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. your attention to detail and understanding of regulatory requirements will be essential in supporting the organization’s commitment to patient safety and compliance. what you will be doing: collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines. conducting signal detection and risk assessment activities to identify potential safety issues. collaborating with cross-functional teams to support safety-related inquiries and investigations. maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices. assisting in the preparation of safety reports and regulatory submissions. your profile: bachelor's degree in life sciences, pharmacy, or a related field; advanced degree preferred. experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical environment. strong analytical skills with attention to detail in data collection and reporting. excellent communication and interper...
Horatio bogota, d.c., capital district, colombia the training manager is responsible for improving the productivity of the organization's employees. this position assesses new clients' developmental needs to drive training initiatives and identifies and arranges suitable training solutions for employees and clients. this position actively searches, creatively designs, and implements effective methods to educate, enhance performance, and recognize performance. responsibilities: develops training and development programs and objectives obtains and /or develops effective training materials utilizing a variety of media trains and coaches managers, supervisors, and others involved in employee development efforts develops and maintains organizational communications such as intranet bulletin boards and newsletters to ensure employees are aware of training and development events and resources conducts follow-up studies of all completed training to evaluate and measure results modifies programs as needed exemplifies the desired culture and philosophies of the organization works effectively as a team member with other members of management and the hr staff required skills/abilities: advanced near-native english proficiency excellent verbal and written communication skills strong presentation skills adept with a variety of multimedia training platforms and methods ability to evaluate and research training options and alternatives ability to design and implement effective training and development on-site role based in bogota. powered by jazzhr i7it...
Latam senior pharmacovigilance analyst page is loaded latam senior pharmacovigilance analyst apply locations bogota, colombia time type full time posted on posted yesterday time left to apply end date: july 11, 2025 (1 day left to apply) job requisition id r1492325 job overview key responsibilities: - team leadership: lead a small local team, providing guidance and support to ensure effective execution of psp activities across latam. - project management: oversee multiple pharmacovigilance projects simultaneously, ensuring timely and accurate reporting of aes. - client audits: conduct face-to-face and remote client audits throughout the year to ensure compliance and address client needs. - kpi metrics: develop and monitor key performance indicators (kpis) for psp support across the region, ensuring targets are met. - adverse event reporting: prepare and deliver detailed ae reports to clients in latam, maintaining high standards of accuracy and clarity. - training and development: provide pharmacovigilance training to team members and other stakeholders involved in the projects. - data review: conduct thorough reviews of data sources generated for each project to identify and report aes. - reconciliation process: manage the reconciliation process for each project, ensuring data consistency and accuracy. - e2e process analysis: analyze the e2e process to identify areas for improvement and implement best practices. - source data verification: perform source data verification to ensure the integrity and accuracy of reviewed data. - cross-functional collaboration: work c...
For project management services. what makes you a fit: the technical part: bachelor of science in engineering (mechanical or electrical) and at least five (5) years of experience in project management within the pharmaceutical industry. shift: administrative, with flexibility based on business needs. bilingual: english and spanish (verbal and written). experience in: project management lifecycle: scope of work, cost estimation, procurement, bidding process, scheduling, project control, contractor supervision, and start-up. managing projects for utilities, fire protection systems, lightning protection, and purified water systems. understanding of pharmaceutical manufacturing processes, regulations, and industry best practices. the personality part: we seek someone who treats everyone like family—our resources, clients, and team members. a customer service-oriented professional with innovative ideas and a commitment to top-quality results. are you ready to be the piece? as a piece of fits, you will: (the day-to-day on the job) manage all aspects of projects: planning, implementation, monitoring, completion, and follow-up. prioritize critical tasks and manage competing timelines. establish and meet project standards for quality and quantity. assess issues and develop solutions to meet scientific, productivity, quality, and client satisfaction goals. research issues, provide recommendations, and maintain documentation to support technical, financial, and organizational decisions. maintain and track project budgets. allocate and reconcile resources effectively. identify schedule...
Join amgen’s mission of serving patients at amgen, if you feel like you’re part of something bigger, it’s because you are. our shared mission—to serve patients living with serious illnesses—drives all that we do. since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. with our focus on four therapeutic areas –oncology, inflammation, general medicine, and rare disease– we reach millions of patients each year. as a member of the amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. our award-winning culture is collaborative, innovative, and science based. if you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the amgen team. join us and transform the lives of patients while transforming your career. commercial pricing manager ( bogotá) what you will do let’s do this. let’s change the world. in this vital role you will a strategic and results-driven pricing manager to join our team in colombia, focusing on the pharmaceutical and biotechnology sectors. this critical role will be responsible for designing, implementing, and monitoring pricing strategies that align with business objectives, ensure regulatory compliance, and strengthen our competitive position in the market. the pricing manager will collaborate with cross-functional teams to drive profitability and optimize pricing models for innovative therapies and pharmaceutical products: pricing strat...
As a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. as a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. we are seeking a dedicated sr centralized study associate to join our team. the successful candidate will be responsible for: clinical systems & access management: managing clinical systems and access.maintaining study databases (ctms, iwrs, edc, etc.).supporting the study team in data review and other related activities.tracking and following up with cras for outstanding issues.generating study-specific reports.managing internal/external communications.assisting in ensuring training compliance for study teams.managing study payments (site and vendor). data review: following up with cras...
As a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. as a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. we are seeking an experienced and highly motivated centralized study specialist i to join our team. this role involves managing clinical systems, supporting study documentation, ensuring compliance, and providing leadership and mentorship to junior team members. the successful candidate will play a pivotal role in the successful execution of clinical trials and contribute to process improvement initiatives. key responsibilities: clinical systems management: oversee and manage clinical systems.maintain study databases (ctms, iwrs, edc, etc.).support etmf management. study coordination: tr...
Job overview key responsibilities: - team leadership: lead a small local team, providing guidance and support to ensure effective execution of psp activities across latam. - project management: oversee multiple pharmacovigilance projects simultaneously, ensuring timely and accurate reporting of aes. - client audits: conduct face-to-face and remote client audits throughout the year to ensure compliance and address client needs. - kpi metrics: develop and monitor key performance indicators (kpis) for psp support across the region, ensuring targets are met. - adverse event reporting: prepare and deliver detailed ae reports to clients in latam, maintaining high standards of accuracy and clarity. - training and development: provide pharmacovigilance training to team members and other stakeholders involved in the projects. - data review: conduct thorough reviews of data sources generated for each project to identify and report aes. - reconciliation process: manage the reconciliation process for each project, ensuring data consistency and accuracy. - e2e process analysis: analyze the e2e process to identify areas for improvement and implement best practices. - source data verification: perform source data verification to ensure the integrity and accuracy of reviewed data. - cross-functional collaboration: work closely with the ces team to develop and refine processes for reporting aes to clients in latam. - quality assurance: implement and oversee quality assurance measures to ensure the integrity and accuracy of pharmacovigilance data. - regulatory compliance: stay updated on reg...
Job title: pharmacovigilance associate job location: bogotá, bogota, colombia job location type: on-site job contract type: permanent job seniority level: home based icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. we are currently seeking a pharmacovigilance associate to join our diverse and dynamic team. as a pharmacovigilance associate at icon, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. your attention to detail and understanding of regulatory requirements will be essential in supporting the organization’s commitment to patient safety and compliance. what you will be doing: collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines. conducting signal detection and risk assessment activities to identify potential safety issues. collaborating with cross-functional teams to support safety-related inquiries and investigations. maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices. assisting in the preparation of safety reports and regulatory submissions. your profile: bachelor's degree in life sciences, pharmacy, or a related field; advanced degree preferred. experience in pharmacovigilance, drug safety, or a related area, preferably within a clini...
As a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. as a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. we are seeking an experienced and highly motivated senior centralized study specialist to join our team. this role involves managing clinical systems, supporting study documentation, ensuring compliance, and providing leadership and mentorship to junior team members. the successful candidate will play a pivotal role in the successful execution of clinical trials and contribute to process improvement initiatives. key responsibilities: clinical systems management: manage clinical systems, including ctms milestone updates at site/country/protocol levels.manage and review study documents and...
Prestar un servicio de calidad y de apoyo a los clientes externos e internos para reducir las quejas y reclamos. - indagar la solicitud del requerimiento del cliente y dar respuesta inmediata y eficiente de acuerdo al alcance, apoyado en los procesos relacionados. - realizar proceso de corte en sap y solicitar a logística bodega entrega de material para el proceso de adecuación, etiquetado y entrega al cliente. - solicitar tiquetes aéreos y reservas de hotel de acuerdo a itinerario informado; se confirma por medio de correo al asesor comercial. - envío de documentos a gerencia y financiero para realizar análisis financiero y confirmar aprobación de crédito. - solicitud, recepción, validación y archivo de los documentos enviados por los clientes para creación, actualización y reactivación. - seguimiento a liquidaciones, ingresos de material a sap y solicitud de precios para facturar. - instrucción y seguimiento de registros de importación, ica, invima o productos controlados - recepción, revisión, digitalización y entrega al cliente de facturas de importación, exportación, re expedición junto con los demás documentos para los procesos de nacionalización del cliente. - trazabilidad de arribo a bodega de cargas aéreas y marítimas - envío al cliente los documentos de transporte junto con los datos de reserva (sea/ air) para aprobación de despacho previa obtención de los permisos de importación. - atender requerimientos de ventas tipo de puesto: tiempo completo, indefinido salario: $1.300.000 - $1.400.000 al mes consideraciones ante el covid-19: trabajo en casa, a...
Manejo de montacarga, recepción almacenamiento y despacho mercancías, cargue y descargue de contenedores, labores de bodega, verificación de mercancía, ubicación y alistamiento de mercancía, reporte de averías, realizar inventarios, identificación cargas ilícitas, limpieza y adecuación de productos a despachar, limpieza y desinfección de áreas. disposición para trabajo en alturas. tipo de puesto: tiempo completo, indefinido salario: $1.000.000 - $1.000.001 al mes consideraciones ante el covid-19: protocolos de limpieza y desinfección...
Manejo de montacarga, recepción almacenamiento y despacho mercancías, cargue y descargue de contenedores, labores de bodega, verificación de mercancía, ubicación y alistamiento de mercancía, reporte de averías, realizar inventarios, identificación cargas ilícitas, limpieza y adecuación de productos a despachar, limpieza y desinfección de áreas. disposición para trabajo en alturas. tipo de puesto: tiempo completo, indefinido salario: $1.000.000 - $1.000.001 al mes consideraciones ante el covid-19: protocolos de limpieza y desinfección...
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