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 requisit...
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 ...
At johnson & johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity. diversity & inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. regardless of your race, belief, sexual orientation, religion, or any other trait, you are welcome in all open positions at the largest healthcare company in the world. when you join johnson & johnson, your move could mean our next breakthrough. this is a cross-sector role. learn more about our sectors: **medical devices** at johnson & johnson medical devices companies, we are using our breadth, scale, and experience to reimagine the way healthcare is delivered and to help people live longer, healthier lives. in a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics, and interventional solutions with the big ideas of others to design and deliver doctor and patient-centric products and solutions. we are in this for life. we are changing the trajectory of human health, you can too. **pharmaceuticals** at janssen, we’re creating a future where disease is a thing of the past. we’re the pharmaceutical companies of johnson & johnson, working tirelessly to make that future a reality for patients everywhere by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart. we focus...
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,...
**company description**: are you ready to accelerate your career? join cielo as a recruiter! a career at cielo will give you the opportunity to work with the industry’s smartest people and to take ownership of your success! cielo is a brand that reflects our big idea - that talent is rising - and with it our opportunity to rise above. we create careers for ambitious people by moving beyond traditional assumptions of what it means to work in talent acquisition. cielo is the world's leading talent acquisition partner. we deliver a better talent experience for everyone through talent acquisition, search, consulting, and digital accelerators. with our fresh approach - we design and build comprehensive, proven solutions inspired by technology to find and keep the unique talent that elevates our clients above the competition. **work arrangemente**:remote **language requirements**:fluent in english and spanish **specific needs**:recruitment experience in the pharmaceutical sector **responsibilities**: - solicit and pursue referrals from business networks and/or internal referrals. - issue skills testing as needed and evaluate results (if process dictates). - review background and reference information (if process dictates). - partner with hiring leader to determine offer details, using market data and compensation guidelines to support recommendations. - service excellence: - strict adherence to all regulations (ofccp and all other compliance standards set forth). - provide accurate and regular reporting of recruiting activities to the hiring leader and cielo l...
Caring for the world, one person at a time has inspired and united the people of johnson & johnson for over 125 years. we embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. with $82.1 billion in 2020 sales, johnson & johnson is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices markets. employees of the johnson & johnson family of companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. if you have the talent and desire to touch the world, johnson & johnson has the career opportunities to help make it happen. thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. proud to be an equal opportunity employer. johnson & johnson is the world's most comprehensive and broadly-based healthcare company, touching the lives of nearly a billion people every day. our family of companies throughout the world compete in consumer, pharmaceutical and medical devices & diagnostics markets and have the skills and resources to tackle the world's most pressing health issues. - _ nchc is recruiting for a gs strategy director with their global services organization global services is the global shared services organization supporting multifunctional services delivery. they perform select functional work in a consistent manner across regions using simplified, standa...
As clinical research associate (cra), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. a cra is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. you will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **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. -...
Caring for the world, one person at a time has inspired and united the people of johnson & johnson for over 125 years. we embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. with $82.1 billion in 2020 sales, johnson & johnson is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices markets. employees of the johnson & johnson family of companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. if you have the talent and desire to touch the world, johnson & johnson has the career opportunities to help make it happen. thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. proud to be an equal opportunity employer. johnson & johnson is the world's most comprehensive and broadly-based healthcare company, touching the lives of nearly a billion people every day. our family of companies throughout the world compete in consumer, pharmaceutical and medical devices & diagnostics markets and have the skills and resources to tackle the world's most pressing health issues. - _ nchc is recruiting for a gs strategy director with their global services organization global services is the global shared services organization supporting multifunctional services delivery. they perform select functional work in a consistent manner across regions using simplified, standa...
**job description**: our clinical research and pharmacovigilance team push the boundaries of global healthcare through research and innovation. through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. **position overview**: under the direction of the applicable management, the clinical data manager is responsible for executing end to end data management activities pertaining to clinical trials, including but not limited to; data management tool and system development, validation and maintenance, data collection, data integrity review and reconciliation, query management, medical coding, and database lock preparation, in compliance with our company standard operating procedures and guidelines. **primary activities include, but are not limited to**: - receives the study related paper documents from sites or other functional areas, and transfers to data entered for processing. - performs sponsor data entry as applicable per data management plans following entry guidelines. - participates in the development and change request implementation of data management tools and systems for the clinical trial data management activities - execute data validation activities in accordance with relevant standard operating procedures. - raises questions to investigational site staff and internal and external vendors, reviews responses and corresponding data corrections to confirm identified issue resolution. - responsible for the execution of user acceptance testing of data m...
As a senior regulatory affairs specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. the senior regulatory affairs associate has responsibility for providing comprehensive regulatory services to clients within the pharmaceutical, biologic, medical device or other regulatory services environments. this will include support for assessment, registration, maintenance and other activities as assigned. you will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. working in this program you will feel challenged and supported to advance in your professional career while making a truly impact. **what you will be doing**: the regulatory affairs specialist will be working with drugs' registration according to the local regulatory agencies. - perform all electronic submissions of registration and post-registration requests to regulatory agencies. - ensure all expected/required correct data is updated/ uploaded in the systems (veeva) - supports assigned teams in the preparation of all submission types in adherence with applicable legislation, regulations and guidelines facilitating approvals and continued client compliance. - maintains a positive and productive liaison with internal and external contacts. this may include clients, regulatory agencies, and related institutions. - assists in the development of assessments and strategic regulatory plans for client product development programs. supports the develo...
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 science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **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. - may be assigned clinical tasks where advanced negotiating skills are required. **you are**: - bachelor’s degree in a health, life sciences or other relevant field of study. ...
Management assistant - colombia, bogota hybrid: office/remote 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 management assistant office based role (hybrid) - mexico city, mexico - bogotá, colombia icon plc is a world-leading healthcare intelligence and clinical research organisation. from molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. with our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. our people are our greatest strength, are at the core of our culture, and the driving force behind our success. icon people have a mission to succeed and a passion that ensures what we do, we do well. the role: as a management assistant at icon, your job is essential in latam regional support across all divisions (ibt, ipd, iod, idc), supporting the regional leadership governance meetings and actions, capabilities & country input for sales/pm/feasibility/ssu, etc. this is a role that responds to the special requirement and needs for the region to have a governance and oversight that helps the global services be able to receive information on latam and respond to growth in the region for clinical operations this support includes quality...
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 science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **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. - may be assigned clinical tasks where advanced negotiating skills are required. **you are**: - bachelor’s degree in a health, life sciences or other relevant field of study. ...
Compañía comercializadora de insumos y material de empaque para el sector farmacéutico requiere un tecnólogo en comercio exterior o carreras a fines de negocios internacionales, con experiência de uno a dos años, recién egresado con ganas de aprender, persona proactiva, analítica y buena actitud de servicio, con nível de ingles medio, escrito, para apoyo al proceso de compras. tipo de puesto: tiempo completo salario: $1.300.000 - $1.500.000 al mes consideraciones ante el covid-19: medidas básicas de limpieza y desinfección, uso tapabocas opcional, trabajo en casa...
Compañía comercializadora de insumos y material de empaque para el sector farmacéutico requiere un tecnólogo en comercio exterior o carreras a fines de negocios internacionales, con experiência de uno a dos años, recién egresado con ganas de aprender, persona proactiva, analítica y buena actitud de servicio, con nível de ingles medio, escrito, para apoyo al proceso de compras. tipo de puesto: tiempo completo salario: $1.300.000 - $1.500.000 al mes consideraciones ante el covid-19: medidas básicas de limpieza y desinfección, uso tapabocas opcional, trabajo en casa...
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 p...
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....
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