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. our global clinical department consists of colleagues with institutional knowledge, in-depth therapeutic experience, and robust operational tools. together, we help clients define and develop clinical programs, minimize delays and execute high-quality, cost-efficient clinical studies. as a ppd cra, you will perform and coordinate all aspects of the clinical monitoring and site management process. 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: essential functions: - 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 wri...
**job description**: 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. our global clinical department consists of colleagues with institutional knowledge, in-depth therapeutic experience, and robust operational tools. together, we help clients define and develop clinical programs, minimize delays and execute high-quality, cost-efficient clinical studies. as a ppd cra, you will perform and coordinate all aspects of the clinical monitoring and site management process. 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: essential functions: - 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...
**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 clinical research services — 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 department consists of colleagues with institutional knowledge, in-depth therapeutic experience, and robust operational tools. together, we help clients define and develop clinical programs, minimize delays and execute high-quality, cost-efficient clinical studies. as an **assistant cra (acra)**, you combine knowledge, therapeutic expertise, and robust tools to help our clients deliver life-changing therapies to market. you take ownership, anticipate problems, find solutions, and deliver results. at ppd clinical research services 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 remote activities on assigned projects in liaison with the remote cra, on-site cra and study ctm. provides support with regards to site preparedness, logístical support to the monitoring process, and assist with assigned tasks for site management and remote monitoring in accordance with sops and regulatory guidelines. may be assigne...
**summarized purpose**: 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 (i.e. fso, fsp, government, etc.). acts as a site processes specialist, ensuring that the trial **essential functions** - 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 payment process. ensures a shared responsibility with other project team members on issue...
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 include: general medicine. **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 clinical deliverables, anticipates problems, finds solutions and delivers results. **a day in the life of a ctm**: - ...
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 include: general medicine. **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 clinical deliverables, anticipates problems, finds solutions and delivers results. **a day in the life of a ctm**: - ...
**summarized purpose**: 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 (i.e. fso, fsp, government, etc.). acts as a site processes specialist, ensuring that the trial **essential functions** - 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 payment process. ensures a shared responsibility with other project team members on issue...
Solicitamos portero para trabajar en unidad residencial ubicada cerca a la luis amigó. es para realizar el reemplazo de una incapacidad. se paga el salario mínimo más las prestaciones y seguridad social; promedio quincenas de 900 a 1millon. nota; no debe tener antecedentes o demandas por alimentos no tener malas referencias tener mala actitud. tipo de puesto: tiempo completo...
La agencia de gestión y colocación de empleo comfandi, en alianza con una importante empresa, requiere para su equipo de trabajo: coordinador de calidad – cartago. funciones: - verificar y controlar que los resultados en cada proceso de producción se estén realizando con todas las especificaciones y requerimientos necesarios para asegurar un producto de excelente calidad y velar por el mantenimiento del sistema de gestión de la calidad y gestión humana. requisitos: - profesional ingeniero industrial. - experiencia de 7 meses a 1 año en el cargo. condiciones de la vacante: - salario: $ 1.800.000 a $ 2.000.000. - contrato: fijo. - horario: lunes a viernes de 7:30 am - 5:00 pm. comfandi o sus aliados no solicitan dinero para la consecución, asignación u otra actividad relacionada con las ofertas de empleo, si sospechas de algún fraude infórmanos de inmediato: [email protected]...
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. **discover impactful work**: the principal business information analyst leads discussions with the business to identify key performance metrics to provide insights into performance and is accountable for the timely and accurate production of reports and is allocated as metrics lead to initiatives to implement improvements. in this role you will provide guidance and support for complex ad hoc queries and demonstrate a solid understanding of the industry and associated benchmarks, using this knowledge to provide valuable insight into performance. **a day in the life**: - performs exploratory data analysis to surface data and identify trends. performs review on completed deliverables before sending to customer. - takes ownership for achieving deliverables within the specified time ...
Performs and coordinates all activities required to finalize site contracts (including, contractual terms and conditions, associated investigator grant budget(s) payment schedule terms and conditions, ancillary and site-specific documents), with investigator sites, pharmacies, laboratories or other relevant contractual parties during the lifecycle of the study. reviews ppd and/or client site contract, budget, payment schedule and ancillary documents templates for compliance with local legislation and practices. adapts the site contract template to client and investigational site requirements in collaboration with key stakeholders to include the project team and the ppd legal team. facilitates effective budget negotiation with site personnel in collaboration with key stakeholders. performs and coordinates all amendments to site contracts and financial agreements with investigator sites, pharmacies, laboratories or other relevant contractual parties during the lifecycle of the study. serves as contact with investigative sites for contractual issues and negotiations throughout the lifecycle of a study. assumes responsibility for any ongoing contract or budget amendments....
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 manage 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 global 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. **discover ...
Importante empresa de alimentos está en búsqueda de vendedor mini mercados y autoservicio, con experiência en el área comercial y de ventas de productos de consumo masivo y grandes superficies: **requisitos**: - técnico certificado. - experiência certificada de 2 años en cargos relacionados y de consumo masivo. - 1 año de experiência en el canal autoservicios o mini mercados en compañías de consumo masivo, con manejo de recaudo en efectivo y gestión de cartera - conocimientos solidos en dinámicas de ventas, recaudo, metas mensuales, plan de incentivos y cierre de resultados. - manejo de clientes y portafolio de más de 60 referencias. - manejo de rutas. disponibilidad de viajar cali condiciones: - contrato obra o labor 3 meses reemplazo incapacidad, posibilidad de continuar o pasar directo. - lunes a sábado - fácil traslado dentro de la ciudad. - salario básico fijo$1.300.000 + variable $1.378.000 + auxilio de rodamiento$164.709 + aux. alimentación + aux. transporte + prestaciones de ley. tipo de puesto: tiempo completo salario: $1.300.000 - $2.500.000 al mes experiência: - ventas de productos de consumo masivo: 2 años (obligatorio) - minimercados y autoservicios: 1 año (obligatorio)...
Ppd’s (a part of thermo fisher scientific) 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. our project delivery team directs, coordinates and leads the technical and operational aspects of projects, securing the successful completion of clinical trials. the team is therapeutically aligned to respond better to our customer needs. the therapeutic scope includes general medicine, hematology and oncology (hemonc), infectious and respiratory diseases (ird), cardiovascular, metabolic and critical care (cvmet), neuroscience, vaccines and fsp/client-dedicated. as a clinical team manager (ctm), you combine deep knowledge, therapeutic expertise, and robust tools to help our clients deliver life-changingtherapies to market. you take ownership, anticipate problems, find solutions and deliver results. you take ownership, anticipate problems, find solutions and deliver results; coordinating the activities of clinical management members which are allocated to a project on a regional or country basis. you will work in partnership with the project manager to ensure the necessary training, tracking and quality systems are in place for the clinical management team and be primarily responsible for the clinical deliverables of the project within agreed timelines and budget. clinical team managers p...
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 have an opportunity to join our best in class global feasibility group as an associate feasibility strategist, a senior level position within the team. the role sources and analyzes data to develop site and patient strategies for proposals and post-award feasibility offerings. you will handle pre-award efforts and post-award trial optimization and/or site id assessments. your scope starts at the request for proposal stage through to the end of the feasibility assessment, delivering accurate and robust data-driven strategies to drive a successful study endpoint. travel requirements for the role include attending bid defense meetings once quarterly. essential duties: - develops and presents strategies to clients using modeling tools that mine and aggregate data sources and ...
Roles and responsibilities for the overall success of the proposal development process within the **general medicine** 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 gen med; 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, commercial or...
**summarized purpose**: **essential functions** - 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 payment process. ensures a shared responsibility with other project team members on issues/findings resolution. investigates and follows-up on findings as applicable. - provides trial status tracking and progress update reports to the clinical team. - manager (ctm) as required. ensures study systems are updated per agreed study conventions (e.g. clinical trial management system, ctms). performs qc check of reports generated from ctms system where required. - participates in in...
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 manage 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 global 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. **discover ...
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 manage 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 global 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. **discover ...
**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. 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 ad...
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. discover impactful work: provides administrative safety support to the pharmacovigilance department. specifically in relation to submissions, tracking and subsequent filing and archiving or expedited and periodic safety reports. this includes other general administration tasks such as filing, photocopying, typing and performing reconciliation tasks. involved in projects relating to safety reporting. may mentor or train new central safety reporting admin staff. a day in the life: •responsible for the submission of safety reports to applicable parties, including subsequent scanning, indexing and filing (both electronic and paper), safety tracker completion and quality check, and archiving in accordance with sop’s and wpd’s. resolves simple problems with submission packs within minimal inp...
Looking for caregivers to join our home care family description: at comforcare home care, we value our home care aides like family. we celebrate success and have fun! our focus is to help our clients and employees live their best lives possible. we are searching for experienced caregivers and invite you to become part of our team. we have open positions and are looking for the very best to support clients in their homes. opportunities are located in the following areas: columbia, north east columbia please apply today if you are: 21 years of age or older a licensed, insured driver a reliable and experienced caregiver seeking weekly pay, monthly recognition, continuing paid training, ppd and mileage reimbursement, referral bonuses, paid orientation, and flexible schedules job summary: the caregiver provides clients with personal care and housekeeping services according to an established care plan to help them remain in their residence. essential functions: personal care assistance caring companionship and activities meal planning and preparation assistance with bathing, dressing, grooming, toileting, and incontinent care errands and transportation housekeeping services medication reminders thank you for applying with comforcare of midlands. we look forward to hearing from you! compensation: $10.00 per hour live your best life while helping others live theirs our caregivers are the heart of what we do. we prioritize our caregiversfirst promise, which includes respectful treatment, ongoing training, support in the field, and thoughtful client matching. join our team and be par...
Work schedule standard (mon-fri) environmental conditions office job description 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. discover impactful work: provides administrative safety support to the pharmacovigilance department. specifically in relation to submissions, tracking and subsequent filing and archiving or expedited and periodic safety reports. this includes other general administration tasks such as filing, photocopying, typing and performing reconciliation tasks. involved in projects relating to safety reporting. may mentor or train new central safety reporting admin staff. a day in the life: • responsible for the submission of safety reports to applicable parties, including subsequent scanning, indexing and filing (both electronic and paper), safety tracker completion and quality check, and archiving in accordance with ...
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 unificar y armonizar los procesos para tener un panorama integral de la gestión de las entidades. requisitos experiencia mínima 1 año en planeación y mipg curso de humanización prueba de tuberculina (ppd) esquema de vacunas requerido completo y al día condiciones laborales ibc $1.423.500 + aux. movilidad $1.206.146 horarios administrativos: lun-jue 7:30 - 5:30, viernes hasta las 4:30, sábados ocasionalmente si el área lo requiere. candidatos interesados y quienes cumplan con los requisitos aplicar con hoja de vida adjunta. nota: favor tener en cuenta que solo se consideran las hojas de vida que cumplan con la experiencia y requisitos requeridos. #j-18808-ljbffr...
Join to apply for the proj mgr clin supplies role at thermo fisher scientific continue with google continue with google join to apply for the proj mgr clin supplies role at thermo fisher scientific work schedule standard (mon-fri) 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. the role we are seeking an associate project/project manager to join our global clinical supplies team. this can be office based, hybrid, or fully homebased. a day in the life this role provides complete oversight of supply chain for sophisticated global clinical trials. ensures project/study activities are in compliance with company and client requirements and acts as a representative for the department on all assigned projects. key responsibilities: develops study specific plans for ...
Cree una alerta de empleo y reciba nuevas ofertas que se adaptan a su perfil desde más de 2550 sitios web de empleo