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Médecins sans frontières is an international independent medical-humanitarian organization that offers assistance to populations in distress, victims of natural or man-made disasters, and victims of armed conflict, without discrimination and irrespec...
At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. our global clinical operations colleagues within our ppd clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. together, we help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies. discover impactful work: performs and coordinates all aspects of the clinical monitoring and site management process. conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. manages procedures and guidelines from different sponsors and/or monitoring environments ( fso, fsp, government, etc.). acts as a site processes specialist, ensuring that the trial is con...
**job description**: we are vital links between an idea for a new medicine and the people who need it. we are the people of ppd — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. you will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. are you a data and a people person? here’s your team. we manage and clean the data collected in a clinical trial — from the design and build of the database and edit checks, through the entry and cleaning of data to the final delivery of clinical trial data. we work closely with the project teams and clients to identify best practices and processes, meet and exceed our clients’ needs, and do the right thing to earn their trust. as a senior clinical data team lead, you will help ensure the highest quality of data and effectiveness of clinical trail data. you will work directly with cdm pm’s to lead, create, monitor and close studies in a timely manner. this position also works with sites, clients, and other team members at ppd. at ppd we hire the best, develop ourselves and each other, and recognize the power of being one team. we offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. summarized purpose: acts as a lead data manager for one or more projects and a liaison to the pm and /or client as required. essential functions: - acts as an interdepartmental and client liaison for all...
**job description**: we are vital links between an idea for a new medicine and the people who need it. we are the people of ppd — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. you will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. are you a data and a people person? here’s your team. we manage and clean the data collected in a clinical trial — from the design and build of the database and edit checks, through the entry and cleaning of data to the final delivery of clinical trial data. we work closely with the project teams and clients to identify best practices and processes, meet and exceed our clients’ needs, and do the right thing to earn their trust. as a senior clinical data associate, you will help ensure the highest quality and effectiveness of clinical trial data. you will work directly with team members to clean and edit clinical trial data in a timely manner. you will also work with edc(electronic data capture) systems and process study specific reports and data listings. at ppd we hire the best, develop ourselves and each other, and recognize the power of being one team. we offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. summarized purpose: performs all aspects of the data cleaning process, with mínimal supervision, in accordance with gcp and sops/wpds in order to assess the safety and efficacy ...
We are vital links between an idea for a new medicine and the people who need it. we are the people of ppd — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. you will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. our **global clinical supplies** team cover all aspects from purchasing to global inventory management and from distribution to destruction. we have a new vacancy for **project manager/senior project manager** (depending on experience) for our **global clinical supplies team** to be based in the **latam** **region**. this can be office based or home based. **key responsibilities**: a project manager (pm) in the gcs team is responsible for providing overall global coordination of the entire clinical supplies lifecycle for the projects assigned. also responsible for managing the more complex clinical supplies studies. these studies require primary and/or secondary packaging and labelling design, drug projections, drug distribution and returns, drug inventory management, budgeting and developing project specific material for multiple projects at the same time. the pm provides consultation services to clients regarding global packaging, labelling, and distribution requirements. this person also serves as the main point of contact between the client, clinical project teams, third party vendors, and study sites. **education and experience**: - bachelor's degree in a science or related disci...
**job description**: we are vital links between an idea for a new medicine and the people who need it. we are the people of ppd — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. you will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. are you a data and a people person? here’s your team. we manage and clean the data collected in a clinical trial — from the design and build of the database and edit checks, through the entry and cleaning of data to the final delivery of clinical trial data. we work closely with the project teams and clients to identify best practices and processes, meet and exceed our clients’ needs, and do the right thing to earn their trust. as a manager clinical data management, you will help ensure the success of your team and cdm projects. you will work to provide training, mentorship and guideance. this includes but not limited to interviewing new staff, performance management, reviewing and approving time and expense reports. at ppd we hire the best, develop ourselves and each other, and recognize the power of being one team. we offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. summarized purpose: manages project staff and workload of direct reports. responsible for training, mentoring, and guiding project staff and direct reports within a portfolio. essential functions: - manages staff...
Bairesdev is proud to be one of the fastest-growing companies in latin america and a welcoming, highly rated employer (glassdoor employee score: 4.3). with more than 3500 employees in 27 countries and world-class clients from start-ups to fortune 500 companies, we’re only as strong as the multicultural teams at the heart of our business. bairesdev runs on talent. to consistently deliver the highest quality solutions to our clients, we only hire the top 1% of it talent and nurture their professional growth on exciting projects for companies like google, pinterest, and udemy. we are looking for a sales manager to lead our sales team and help spearhead our growth. as a sales manager, you will play a critical and active role in the day-to-day operations. this is an excellent opportunity to be one of the key members of our sales team and position yourself for unique career growth opportunities. main activities: - achieve growth and hit sales targets by successfully managing the sales team. - provide complete and appropriate solutions to boost revenue growth and profitability. - design and implement strategic business plans. - establish, develop, and maintain positive business and customer relationships. - own recruiting, objectives setting, coaching and performance monitoring of sales representatives. what are we looking for: - proven work experience as a sales manager. - must be highly motivated, flexible, and service-oriented. - must be familiar with crm practices, along with the ability to build productive business professional relationships. - goal-oriented,...
Importante empresa de la región con el apoyo de la agencia de empleo de comfenalco santander, requiere persona con formación básica primaria o bachiller, con mínimo 4 años de experiencia como empleado/a servicio doméstico interna/o, con conocimientos en limpieza y aseo general, preparación de alimentos, lavado de ropa y servicio al cliente. indispensable: saber cocinar. lugar de trabajo: ruitoque condominio horarios: lunes a sÁbado 46 horas , dÍa de salida sÁbado, dÍa ingreso domingo. salario: $ 1.723.500 + prestaciones de ley. tipo de contrato: término fijo funciones ? mantener limpio y aseado las áreas asignadas. ? clasificar las basuras en desechos orgánicos e inorgánicos. ? preparar y manipular alimentos. ? realizar el lavado y doblado de prendas de vestir. responder por los elementos entregados en el cargo e informar sobre algún deterioro que presente. ? brindar un servicio con respeto, cordialidad y compromiso. ? las demás funciones asignadas por su jefe inmediato de acuerdo a la naturaleza de su cargo....
Roles and responsibilities for the overall success of the proposal development process within the **hematology / oncology **team space; from rfp receipt through client decision. provides leadership and ownership of operational strategies, bid defense hand=off, and accountability for all related operational proposal deliverables, resulting in an increased rfp hit rate, and positive business growth. leverages all opportunities to achieve targets while enhancing customer relations. primarily responsible for rfps and supplemental documents for complex, multi-region, multi-service clinical development projects/programs, partnership and prospective selling initiatives and related client deliverables. converts commercial win strategy into operational strategy that maximizes rfp hit rate resulting in business growth for hemonc; determines the level of proposal deliverable and key operations messages and supports the triage process within clinical operations to meet proposal deliverables. ensures budget reflects operational strategy and manages operations proposal deliverable in order to achieve ppd profitability targets. collaborates with therapeutic and cross functional leadership team to assess success and profitability and ability to execute to plan, assessing process and bidding algorithms. drives the development of the operations segment of the proposal deliverable within prescribed timelines, disseminates operational strategy to proposal team and develops kpi's, ensuring a successful operations segment of the deliverable. partners with clinical operations, commercia...
We are vital links between an idea for a new medicine and the people who need it. we are the people of ppd — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. you will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. ppd’s data analytics programming group supports the centralized monitoring organization in delivering new approaches to risk surveillance and centralized statistical monitoring. we create the data reports, data visualization, tools, and utilities the centralized monitoring group uses to monitor and manage clinical study data to proactively identify risks in a clinical trial. these tools provide insight into things like: - data errors, deviations - trends, outliers - unusual variation (or lack of variation) - potential data manipulation, fraud - other systematic errors or data integrity issues. as a data analytics programmer, you’ll be mapping data, creating custom reports, creating custom visualizations/dashboards, and creating other specialized tools and utilities used in centralized statistical and risk surveillance activities on assigned trials. at ppd we hire the best, develop ourselves and each other, and recognize the power of being one team. we offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. **summarized purpose**: computer programming position working with and integrating data from a var...
**work schedule** standard (mon-fri) **environmental conditions** office **principal trial strategy** at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. roles and responsibilities for the overall success of the proposal development process within the operational strategy unit; from rfp receipt through client decision. **a day in the life of a principal trial strategy**: - provides leadership and ownership of operational strategies, bid defense hand=off, and accountability for all related operational proposal deliverables, resulting in an increased rfp hit rate, and positive business growth. - leverages all opportunities to achieve targets while enhancing customer relations. - primarily responsible for rfps and supplemental documents for complex, multi-region, multi-service clinical development projects/programs, partne...
**work schedule** other **environmental conditions** office at thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.**location/division specific information**: our project delivery colleagues within ppd® clinical research services direct, coordinate and manage the technical and operational aspects of projects, securing the successful completion of clinical trials. through our diverse team, our members engage in variety of initiatives and projects, or are part of global project teams gaining cross-cultural experience. therapeutic scope includes **neurosciences - **rare disease/als/ ophthalmology or psychiatr**y.** **discover impactful work**: the clinical team manager (ctm) combines deep knowledge, therapeutic expertise, and robust tools to help our clients deliver life-changing therapies to market. the ctm takes ownership of cli...
**job description**: we are vital links between an idea for a new medicine and the people who need it. we are the people of ppd — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. you will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. are you a data and a people person? here’s your team. we manage and clean the data collected in a clinical trial — from the design and build of the database and edit checks, through the entry and cleaning of data to the final delivery of clinical trial data. we work closely with the project teams and clients to identify best practices and processes, meet and exceed our clients’ needs, and do the right thing to earn their trust. as a senior clinical data associate, you will help ensure the highest quality and effectiveness of clinical trial data. you will work directly with team members to clean and edit clinical trial data in a timely manner. you will also work with edc(electronic data capture) systems and process study specific reports and data listings. at ppd we hire the best, develop ourselves and each other, and recognize the power of being one team. we offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. summarized purpose: performs all aspects of the data cleaning process, with mínimal supervision, in accordance with gcp and sops/wpds in order to assess the safety and efficacy ...
At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. we are currently seeking a senior regulatory affairs specialist to join our global regulatory affairs department – regulatory science team. this is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting. in this role you will be a pivotal team member with regulatory affairs responsibilities, leading discussions, and coordinating regulatory strategies globally on assigned (phase 1 to 4) clinical trials, studies and projects. you will be part of a global team providing innovative solutions and global regulatory expertise, being client interfacing to provide strategic regulatory intelligence and guidance. you will feel confident providing regulatory advice and carry out projects in the provision of regulatory affairs services whil...
**job description**: we are vital links between an idea for a new medicine and the people who need it. we are the people of ppd — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. you will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. our goal-driven teams combine and deliver startup activities for the clinical trials, collaborating to improve processes, cycle and flexibility. we partner with our sites, businesses and colleagues around the world to decrease startup timelines and exceed expectations. as a country approval specialist, you will be responsible for pulling regulatory country submissions together in order to activate investigative sites. at ppd we hire the best, develop ourselves and each other, and recognize the power of being one team. we offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. summarized purpose: as a country approval specialist, you are responsible for pulling regulatory country submissions together in order to activate investigative sites. you have a strong attention to detail, taking ownership of the accuracy of these documents while holding yourself and others accountable. essential functions: - provides, under guidance local regulatory strategy advice (moh &/or ec) to internal clients - provides project specific local sia services and coordination of these projects - may have c...
**job description**: description - external ppd’s mission is to improve health. it starts as an idea to find a cure. it becomes a life saved. all in-between, it’s you! we know that meaningful results not only require the right approach, but also the right people. we invite you to re-imagine health promoting protocols with us, working alongside our talented, bright, and energetic teams. from purchasing to global inventory management and from distribution to destruction, ppd’s integrated global clinical supplies (gcs) services are designed to increase speed and efficiency, without sacrificing the quality you expect. a vendor mgmnt coordinator provides support to clinical supplies operations and administrative activities in all areas of clinical supplies lifecycle of low to moderate complexity studies. **activities** - actively participates in global project calls and lead discussions on assigned supply chains and liaises with global supply vendors. - makes global purchases (must have), global distributions and deposit processes. - oversees post-sale services and process distribution. - must poses a solid understanding of the clinical supply process, such as manufacturing, handling, importing, shipping, exporting, auditing, labeling, and packaging - previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years). - ensures all activities are executed in compliance with company good practices and client requirements. **job qualification**: **requirements**: - high / secondary school diploma or equiva...
**work schedule** standard (mon-fri) **environmental conditions** office **qualifications**: education and experience: bachelor's degree in a life sciences related field or a registered nursing certification or equivalent and relevant formal academic / vocational qualification. previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor) or completion of ppd drug development fellowship. valid driver's license where applicable. **essential functions and other job information**: monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (rca), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. ensures data accuracy through sdr, sdv and crf review as applicable through on-site and remote monitoring activities. assess investigational product through physical inventory and records review. documents observations in reports and letters in a timely manner using approved business writing standards. escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. may need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. conducts monitoring tasks in accordance with the approved mo...
At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. **location/division specific information**: our project delivery colleagues within ppd® clinical research services direct, coordinate and lead the technical and operational aspects of projects, securing the successful completion of clinical trials. through our diverse team, our members engage in variety of initiatives and projects, or are part of global project teams gaining cross-cultural experience. therapeutic scope include**:the therapeutic scope includes general medicine**-** dermatology, gi, (uc/cd), cardiovascular, liver, nephrology, immunology, rare disease, diabetes, obesity, dyslipidemia, women's health, rheumatology, (ra, sle, gout) **discover impactful work**: the (sr.) clinical team manager (ctm) combines deep knowledge, therapeutic expertise, and robust tools to he...
At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. oversees a qa team responsible for bids, proposals, and budget estimates for billable good clinical practice and good manufacturing practice quality services. manages and develops staff. ensures delivery of quality solutions in a collaborative cross-functional environment. leads process improvement initiatives and communicates with internal operations regarding continuous improvements. - leads the pre - and post-contract management team within the ppd quality and enterprise learning - participates in managing the development of proposals for billable good clinical practice and good manufacturing practice quality services - reviews requests for proposal (rfps) and participates in budget strategy meetings - prepares thorough and accurate written bids, proposals, and budget estimate...
**qualifications**: education and experience: bachelor's degree in a life sciences related field or a registered nursing certification or equivalent and relevant formal academic / vocational qualification. previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor) or completion of ppd drug development fellowship. valid driver's license where applicable. **essential functions and other job information**: - monitors investigator sites with a risk-based monitoring approach: applies root - cause analysis (rca), critical thinking and problem-solving skills to identify site - processes failure and corrective/preventive actions to bring the site into - compliance and decrease risks. ensures data accuracy through sdr, sdv and - crf review as applicable through on-site and remote monitoring activities. - assess investigational product through physical inventory and records review. - documents observations in reports and letters in a timely manner using - approved business writing standards. escalates observed deficiencies and issues - to clinical management expeditiously and follow all issues through to resolution. - may need to maintain regular contact between monitoring visits with - investigative sites to confirm that the protocol is being followed, that previously - identified issues are being resolved and that the data is being recorded in a - timely manner. conducts monitoring tasks in accordance with the approved - monitoring plan. participates in the investigator paym...
**work schedule** standard (mon-fri) **environmental conditions** office **qualifications**: education and experience: bachelor's degree in a life sciences related field or a registered nursing certification or equivalent and relevant formal academic / vocational qualification. previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor) or completion of ppd drug development fellowship. valid driver's license where applicable. **essential functions and other job information**: monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (rca), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. ensures data accuracy through sdr, sdv and crf review as applicable through on-site and remote monitoring activities. assess investigational product through physical inventory and records review. documents observations in reports and letters in a timely manner using approved business writing standards. escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. may need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. conducts monitoring tasks in accordance with the ...
At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. our project delivery colleagues within our ppd® clinical research services direct, coordinate and lead the technical and operational aspects of projects, securing the successful completion of clinical trials. this includes collaborating with functional area leads to identify and evaluate fundamental issues on the project and to ensure that solutions are implemented. project delivery is vital to helping our customers deliver life-changing therapies. through our distributed team, you may engage in diverse initiatives and projects, or be part of a virtual international project team gaining cross-cultural experience. therapeutic scopes include: infectious and respiratory diseases, oncology/hematology, neurosciences, cardiovascular and metabolic, general medicine and vaccines. **discov...
Reconocida ips busca personas con talento, alta disposición al servicio, con deseos de continuar aprendiendo y creciendo: requerimos profesional de enfermería apoyo nacional, en la ciudad de bogotá con disponibilidad de viajar a nivel nacional, con experiencia mínimo de 1 año en el área de salud, con estudios como profesional de enfermería y experiencia en atención integral de personas con vih, enfermedades renales crónicas, entre otras. para realizar verificación del cumplimiento y la aplicación de la atención vigente en cuanto al manejo y consejería del paciente, asistencia a pacientes, seguimiento y otras. con conocimientos en herramientas ofimáticas e historias clínicas, ofrecemos contrato directo por la empresa, a término indefinido, horarios lunes a sábados, apoyo en gestiones nacionales. debe contar con los siguientes requisitos: • disponibilidad de viajar a nivel nacional • curso de atención a víctimas de violencia sexual • curso de bls • curso de toma de citología cervicouterina • curso de aplicación de ppd promovemos un lugar de trabajo en donde te sentirás respaldado/a, podrás asegurar tu éxito y el bienestar de nuestros usuarios. gracias por tu interés en ser parte de nuestra empresa, valoramos tu candidatura, ¡te deseamos mucho éxito en el proceso! con la aplicación de la hoja de vida está dando autorización para el manejo de datos personales, de acuerdo con lo dispuesto en la ley 1581 de 2012, "por el cual se dictan disposiciones generales para la protección de datos personales" y de conformidad con lo señalado en el decreto 1377 de 2013....
Reconocida ips busca personas con talento, alta disposición al servicio, con deseos de continuar aprendiendo y creciendo: requerimos profesional de enfermería apoyo nacional, en la ciudad de bogotá con disponibilidad de viajar a nivel nacional, con experiencia mínimo de 1 año en el área de salud, con estudios como profesional de enfermería y experiencia en atención integral de personas con vih, enfermedades renales crónicas, entre otras. para realizar verificación del cumplimiento y la aplicación de la atención vigente en cuanto al manejo y consejería del paciente, asistencia a pacientes, seguimiento y otras. con conocimientos en herramientas ofimáticas e historias clínicas, ofrecemos contrato directo por la empresa, a término indefinido, horarios lunes a sábados, apoyo en gestiones nacionales. debe contar con los siguientes requisitos: • disponibilidad de viajar a nivel nacional • curso de atención a víctimas de violencia sexual • curso de bls • curso de toma de citología cervicouterina • curso de aplicación de ppd promovemos un lugar de trabajo en donde te sentirás respaldado/a, podrás asegurar tu éxito y el bienestar de nuestros usuarios. gracias por tu interés en ser parte de nuestra empresa, valoramos tu candidatura, ¡te deseamos mucho éxito en el proceso! con la aplicación de la hoja de vida está dando autorización para el manejo de datos personales, de acuerdo con lo dispuesto en la ley 1581 de 2012, "por el cual se dictan disposiciones generales para la protección de datos personales" y de conformidad con lo señalado en el decreto 1377 de 2013....
Ppd’s mission is to improve health. it starts as an idea to find a cure. it becomes a life saved. all in-between, it’s you! we know that meaningful results not only require the right approach, but also the right people. we invite you to re-imagine health promoting protocols with us, working alongside our hardworking, bright and energetic teams. from purchasing to global inventory management and from distribution to destruction, ppd’s integrated global clinical supplies (gcs) services are designed to increase speed and efficiency, without sacrificing the quality you expect. as a project manager in clinical supplies, you will be r esponsible for providing overall global coordination of the entire clinical supplies lifecycle for the projects assigned. responsible for leading the more complex clinical supplies studies. at ppd we hire the best, develop ourselves and each other, and recognize the power of being one team. we offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. summarized purpose: responsible for providing overall global coordination of the entire clinical supplies lifecycle for the projects assigned. responsible for running the more complex clinical supplies studies. these studies require primary and/or secondary packaging and labeling design, drug projections, drug distribution and returns, drug inventory management, budgeting and developing project specific material for multiple projects at the same time. provides consultation services to clients regarding global packaging, la...
At thermo fisher scientific, you’ll discover meaningful work that makes a positive impact on a global scale. join our colleagues in bringing our mission to life - enabling our customers to make the world healthier, cleaner and safer. we provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. we are currently seeking a senior regulatory affairs specialist to join our growing regulatory affairs department - regulatory liaison team. this is a fantastic opportunity to further your regulatory career and develop your expertise in this field. **senior regulatory affairs specialist - reg liaison** in this role you will be a pivotal team member with ideally with regulatory experience. you will provide innovative solutions including global regulatory therapeutic area expertise and client interface to provide strategic regulatory intelligence, guidance and regulatory expertise for product development from preclinical through registration and product optimization. you will feel confident providing regulatory advice and carry out projects in the provision of regulatory affairs ser...
El hospital departamental mario correa rengifo, requiere para su equipo de trabajo: ingeniero industrial con experiencia mínima de 1 año en mipg, cuyo objetivo principal es guiar a los servidores públicos en la gestión institucional, buscando unifica...
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