Direct message the job poster from clinirx join clinirx: shape the future of global clinical research are you ready to make a significant impact in the world of clinical trials? clinirx, a leading global contract research organization (cro), is expan...
Viseven group is a leading global b2b martech service provider, empowering pharma and lifescience companies since 2009. our mission is to drive digital transformation and excellence, offering comprehensive end-to-end software and digital marketing se...
Comercializadora de insumos y material de empaque para el sector farmaceutico, requiere tecnico, tecnologo o estudiante de programas académicos administrativos, ingenierias, o relacionados, para trabajar de lunes a viernes de 7am a 5pm de manera presencial en zona franca fontibón. algunas funciones a cargo: elaboración, actualización y control de todos los documentos del sistema de gestión de calidad. seguimiento, análisis y generación del informe ejecutivo de los indicadores de gestión de la organización. acompañamiento durante las auditorías externas realizadas por los clientes. tabulación, seguimiento de las no conformidades de la organización emitidas durante las auditorías internas y externas, quejas y reclamos. implementación y verificación de cierre de las acciones correctivas derivadas de las no conformidades. gestionar el manejo de tirillas de los residuos ambientales de la compañía (alimentar cuadro de excel, solicitud de cumplimiento y control de los datos entregados en cada gestor). entre otros. experiência en manejo de sistemas de gestión de calidad iso, u otros. tipo de puesto: tiempo completo salario: $1.300.000 - $1.500.000 al mes consideraciones ante el covid-19: protocolos de limpieza y desinfección....
Comercializadora de insumos y material de empaque para el sector farmaceutico, requiere tecnico, tecnologo o estudiante de programas académicos administrativos, ingenierias, o relacionados, para trabajar de lunes a viernes de 7am a 5pm de manera presencial en zona franca fontibón. algunas funciones a cargo: elaboración, actualización y control de todos los documentos del sistema de gestión de calidad. seguimiento, análisis y generación del informe ejecutivo de los indicadores de gestión de la organización. acompañamiento durante las auditorías externas realizadas por los clientes. tabulación, seguimiento de las no conformidades de la organización emitidas durante las auditorías internas y externas, quejas y reclamos. implementación y verificación de cierre de las acciones correctivas derivadas de las no conformidades. gestionar el manejo de tirillas de los residuos ambientales de la compañía (alimentar cuadro de excel, solicitud de cumplimiento y control de los datos entregados en cada gestor). entre otros. experiência en manejo de sistemas de gestión de calidad iso, u otros. tipo de puesto: tiempo completo salario: $1.300.000 - $1.500.000 al mes consideraciones ante el covid-19: protocolos de limpieza y desinfección....
At claire joster, we are seeking a highly motivated and experienced candidate to join the dynamic drug discovery & mechanism of action (moa) in oncology research team within pharmamar, a leading pharmaceutical company. the successful candidate will play a key role in advancing drug discovery efforts and elucidating the mechanisms of action of novel anticancer agents. this position requires a strong background in cancer biology, molecular biology techniques, and gene editing, along with a proven track record of innovative research. key responsibilities: ensure the successful execution of assigned projects within the required timelines and in accordance with departmental dynamics (e.g., experimental design, assay scheduling, and results review). perform research activities following established internal departmental guidelines and company-wide regulations (e.g., information management, safety protocols). maintain accurate and up-to-date documentation, including results review, data recording in laboratory notebooks and databases. prepare study protocols, activity summaries, project updates, and technical reports. provide intellectual and technical contributions to both individual and team projects, including study proposals, experimental design, and critical review of results. facilitate effective internal communication with team members, other research groups within the department, and cross-functional teams in the r&d division. actively participate in activities that contribute to the efficient operation of the department and the broader r&d area. supervise, train, and ment...
Requerimos profesional graduado preferiblemente en áreas afines al sector farmacéutico. experiência laboral comercial de 2 años en el sector farmacéutico o relacionados: análisis de mercados, fidelización de clientes, apertura nuevos negocios, ventas del sector y servicio al cliente. toma de decisiones. conocimientos en ofimática. tipo de puesto: tiempo completo, indefinido salario: $200.000.000 - $500.000.000 al mes consideraciones ante el covid-19: desinfección, uso tapabocas, controles...
**practicante de market access** **proposito del rol** takeda es una compañía biofarmacéutica mundial centrada en los pacientes, basada en valores e impulsada por la i+d (innovación y desarrollo), que está comprometida con brindar una mejor salud y un mejor futuro a personas de todo el mundo. estamos buscando una persona que brinde apoyo en las actividades relacionadas con el diseño, elaboración, implementación y seguimiento de herramientas relacionadas con health economic and outcome research, propuestas de valor, pricing, planes de marca, rutas de atención, centros de referencia, cambios normativos y demás actividades involucradas con el área de market access. la posición reporta al market access head y está basada en bogotá, colombia. **desafios en la posiciÓn** - apoyar en el manejo y seguimiento de los archivos e información de brand plan, rutas de atención, centros de referencia, cambios normativos, propuestas de valor a las eps e ips y demás procesos relacionados con el área de market access. - brindar apoyo en la diseño y elaboración de la información requerida para las herramientas de health economic and outcome research. - apoyar en el diseño de comunicación de piezas gráficas y presentaciones. - participar en la elaboración de planes de marca para apoyar a las unidades de negocio/franquicias (gastroenterología, vacunas, enfermedades raras y oncología) desde el área. - liderar un proyecto de estandarización de herramientas y modelos para market access. **a quien buscamos** **experiência y educación** - estudiante de carreras de economía, finanzas inte...
As a ihcra you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies and vaccines for many of the world's most challenging diseases including cancer, cardio-metabolic diseases, alzheimer's and infectious diseases. be ready to work in a solid partnership and an environment driven by innovation and continuous improvement. what you will be doing: an in-house cra (ihcra) is a critical role as in-house cras work independently in the field and are the face of the company in the investigative site community. they are also critical as they represent the customer in the prescribing community. in-house cras are responsible for ensuring that patients' rights and safety are protected and that clinical trials are conducted per regulations and the protocol. performs investigator recruitment activities utilizing phone scripts, questionnaires, study site materials and other tools for use in evaluating investigative sites. utilizes the clinical trial management system (the ctms) to ensure investigator recruitment activities are accurately tracked. performs essential document collection, review, maintenance and close-out activities, ensuring that sponsor and investigator obligations are being met and are in compliance with applicable local regulatory requirements and ich/gcp guidelines. supports investigators and investigative staff in fulfilling obligations with r...
Business area: strategic solutions remote working: office based job description as an in-house clinical research associate (ihcra), you will be joining the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies, and vaccines for many of the world's most challenging diseases including cancer, cardio-metabolic diseases, alzheimer's, and infectious diseases. be ready to work in a solid partnership and an environment driven by innovation and continuous improvement. what you will be doing: an in-house cra (ihcra) is a critical role as in-house cras work independently in the field and are the face of the company in the investigative site community. they are also critical as they represent the customer in the prescribing community. in-house cras are responsible for ensuring that patients' rights and safety are protected and that clinical trials are conducted per regulations and the protocol. performs investigator recruitment activities utilizing phone scripts, questionnaires, study site materials, and other tools for use in evaluating investigative sites. utilizes the clinical trial management system (ctms) to ensure investigator recruitment activities are accurately tracked. performs essential document collection, review, maintenance, and close-out activities, ensuring that sponsor and investigator obligations are being met and are in compliance with applicable local regul...
Compañía comercializadora de insumos y material de empaque para el sector farmacéutico requiere tecnólogo en contaduría graduado o estudiante de últimos semestres de contaduría, con excelente manejo de excel y programas contables. conocimientos y experiência en cuentas por cobrar, cuentas por pagar, facturación, nómina y prestaciones. horario de lunes a viernes de 7am a 5pm, presencial. tipo de puesto: tiempo completo salario: $1.450.000 - $1.500.000 al mes consideraciones ante el covid-19: uso tapabocas, aseo limpieza desinfección instalaciones,...
Comercializadora de insumos y material de empaque para el sector farmacéutico requiere personal bachiller o estudiantes de carreras técnicas para trabajar en cargue y descargue de mercancía, manejo de montacarga, gestión de entregas a clientes, atención al usuario, disponibilidad para trabajo en alturas. horario de lunes a viernes de 6:30am a 5pm. zona franca fontibón, salario mínimo legal vigente, más beneficios corporativos. tipo de puesto: tiempo completo salario: $1.000.000 - $1.000.001 al mes consideraciones ante el covid-19: uso tapabocas, protocolos de higiene y desinfección....
As a ihcra you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies and vaccines for many of the world’s most challenging diseases including cancer, cardio-metabolic diseases, alzheimer’s and infectious diseases. be ready to work in a solid partnership and an environment driven by innovation and continuous improvement. what you will be doing: an in-house cra (ihcra) is a critical role as in-house cras work independently in the field and are the face of the company in the investigative site community. they are also critical as they represent the customer in the prescribing community. in-house cras are responsible for ensuring that patients’ rights and safety are protected and that clinical trials are conducted per regulations and the protocol. performs investigator recruitment activities utilizing phone scripts, questionnaires, study site materials and other tools for use in evaluating investigative sites. utilizes the clinical trial management system (the ctms) to ensure investigator recruitment activities are accurately tracked. performs essential document collection, review, maintenance and close-out activities, ensuring that sponsor and investigator obligations are being met and are in compliance with applicable local regulatory requirements and ich/gcp guidelines. supports investigators and investigative staff in fulfilling obligations with regard t...
As a ihcra you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies and vaccines for many of the world’s most challenging diseases including cancer, cardio-metabolic diseases, alzheimer’s and infectious diseases. be ready to work in a solid partnership and an environment driven by innovation and continuous improvement. what you will be doing: an in-house cra (ihcra) is a critical role as in-house cras work independently in the field and are the face of the company in the investigative site community. they are also critical as they represent the customer in the prescribing community. in-house cras are responsible for ensuring that patients’ rights and safety are protected and that clinical trials are conducted per regulations and the protocol. performs investigator recruitment activities utilizing phone scripts, questionnaires, study site materials and other tools for use in evaluating investigative sites. utilizes the clinical trial management system (the ctms) to ensure investigator recruitment activities are accurately tracked. performs essential document collection, review, maintenance and close-out activities, ensuring that sponsor and investigator obligations are being met and are in compliance with applicable local regulatory requirements and ich/gcp guidelines. supports investigators and investigative staff in fulfilling obligations with regard ...
Business area: strategic solutions remote working: office based job description as an in-house clinical research associate (ihcra), you will be joining the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies, and vaccines for many of the world’s most challenging diseases including cancer, cardio-metabolic diseases, alzheimer’s, and infectious diseases. be ready to work in a solid partnership and an environment driven by innovation and continuous improvement. what you will be doing: an in-house cra (ihcra) is a critical role as in-house cras work independently in the field and are the face of the company in the investigative site community. they are also critical as they represent the customer in the prescribing community. in-house cras are responsible for ensuring that patients’ rights and safety are protected and that clinical trials are conducted per regulations and the protocol. performs investigator recruitment activities utilizing phone scripts, questionnaires, study site materials, and other tools for use in evaluating investigative sites. utilizes the clinical trial management system (ctms) to ensure investigator recruitment activities are accurately tracked. performs essential document collection, review, maintenance, and close-out activities, ensuring that sponsor and investigator obligations are being met and are in compliance with applicable local regulator...
Compañía comercializadora de insumos y material de empaque para el sector farmacéutico requiere tecnólogo en contaduría graduado o estudiante de últimos semestres de contaduría, con excelente manejo de excel y programas contables. conocimientos y experiência en cuentas por cobrar, cuentas por pagar, facturación, nómina y prestaciones. horario de lunes a viernes de 7am a 5pm, presencial. tipo de puesto: tiempo completo salario: $1.450.000 - $1.500.000 al mes consideraciones ante el covid-19: uso tapabocas, aseo limpieza desinfección instalaciones,...
Comercializadora de insumos y material de empaque para el sector farmacéutico requiere personal bachiller o estudiantes de carreras técnicas para trabajar en cargue y descargue de mercancía, manejo de montacarga, gestión de entregas a clientes, atención al usuario, disponibilidad para trabajo en alturas. horario de lunes a viernes de 6:30am a 5pm. zona franca fontibón, salario mínimo legal vigente, más beneficios corporativos. tipo de puesto: tiempo completo salario: $1.000.000 - $1.000.001 al mes consideraciones ante el covid-19: uso tapabocas, protocolos de higiene y desinfección....
Business area: strategic solutionsremote working: office basedjob descriptionas an in-house clinical research associate (ihcra), you will be joining the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies, and vaccines for many of the world's most challenging diseases including cancer, cardio-metabolic diseases, alzheimer's, and infectious diseases. be ready to work in a solid partnership and an environment driven by innovation and continuous improvement. what you will be doing: an in-house cra (ihcra) is a critical role as in-house cras work independently in the field and are the face of the company in the investigative site community. they are also critical as they represent the customer in the prescribing community. in-house cras are responsible for ensuring that patients' rights and safety are protected and that clinical trials are conducted per regulations and the protocol. performs investigator recruitment activities utilizing phone scripts, questionnaires, study site materials, and other tools for use in evaluating investigative sites.utilizes the clinical trial management system (ctms) to ensure investigator recruitment activities are accurately tracked.performs essential document collection, review, maintenance, and close-out activities, ensuring that sponsor and investigator obligations are being met and are in compliance with applicable local regulatory r...
Site name: colombia - capital district - bogota posted date: apr 11 2025 your responsibilities: our specialty medical head will be responsible for providing expert scientific capability and leadership while managing a broad range of medical affairs activities associated with his or her assigned products and within the specialty therapy area. this role gives you the opportunity to lead key activities to progress your career, the main of these are: lead the specialty medical area at the local level, collaborating closely with cross-functional and global teams to provide scientific, clinical, and technical expertise, offering guidance and leadership on gsk products.own the external engagement strategy, driving and managing scientific and clinical exchanges with the medical and scientific community to enhance gsk's external presence and reputation.develop and execute a local medical strategic plan for specialty products, ensuring alignment with broader organizational goals and market needs.align with commercial strategic planning, ensuring seamless integration of medical objectives, while managing research budgets and leading the forecasting processes for assigned products and therapeutic areas.provide expert scientific and clinical leadership, offering in-depth knowledge of gsk products and relevant diseases to internal teams and above-country medical networks.foster and elevate scientific knowledge and expertise across the enterprise, ensuring a robust understanding of specialty science, therapeutic trends, and industry advancements.drive excellence in external engagement...
As a ihcra you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a company that is advancing the development of new medicines, biologic therapies and vaccines for many of the world's most challenging diseases including cancer, cardio-metabolic diseases, alzheimer's and infectious diseases. be ready to work in a solid partnership and an environment driven by innovation and continuous improvement. what you will be doing: an in-house cra (ihcra) is a critical role as in-house cras work independently in the field and are the face of the company in the investigative site community. they are also critical as they represent the customer in the prescribing community. in-house cras are responsible for ensuring that patients' rights and safety are protected and that clinical trials are conducted per regulations and the protocol. performs investigator recruitment activities utilizing phone scripts, questionnaires, study site materials and other tools for use in evaluating investigative sites.utilizes the clinical trial management system (the ctms) to ensure investigator recruitment activities are accurately tracked.performs essential document collection, review, maintenance and close-out activities, ensuring that sponsor and investigator obligations are being met and are in compliance with applicable local regulatory requirements and ich/gcp guidelines.supports investigators and investigative staff in fulfilling obligations with regard ...
Rsu specialist for external commerce (comex) location: latam essential functions • responsible for importations and exportation activities in specific latam countries for our fsp model. • ensure adherence to standard operating procedures (sops), work instructions (wis), quality of designated deliverables and project timelines. • perform start up and site activation activities according to applicable regulations, sops and work instructions. distribute completed documents to sites and internal project team members. • ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information. • review and provide feedback to management on site performance metrics. • review, establish and agree on project planning and project timelines. ensure monitoring measures are in place and implement contingency plan as needed. • inform team members of completion of regulatory and contractual documents for individual sites. • provide local expertise to sams and project team during initial and on-going project timeline planning. • perform quality control of documents. • may have direct contact with sponsors on specific initiatives. requirements • clinical research experience. equivalent combination of education, training and experience. • at least 2 years experience related to international trade, import and export processes in pharmaceutical industry • advanced english level • good communicational and interpersonal skills • good organizational skills iqvia is a leading global provider of advanced analytics, technology solution...
We’re looking for people who are determined to make life better for people around the world. manager access position summary: the strategic access manager will be responsible for lead the development and implementation of the access strategy and health economics and outcomes research (heor) for assigned brands. this includes considering cross-functional initiatives aligned with corporate and local strategy, as well as relevant external regulations. key responsibilities: understand the external health environment in the public, political, social and trade sectors. develop and lead cross-functional strategies to enhance access within the national formulary and public institutions. developed value dossiers, value messages, and training field teams. co-create support materials for communication with payers alongside marketing and medical teams. present the value strategy to payers and other relevant stakeholders in the access strategy. monitor and participate in corporate activities to align local strategy with corporate best practices. requirements : professional degree. specialization or mba (health economics, data analytics, epidemiology). 3-5 years of experience in the access field within the pharmaceutical industry. ability to synthesize knowledge and experience for cross-functional project management. strong understanding of the pharmaceutical business, clinical data, and regulatory environment. excellent verbal and written communication skills. work experience in a commercial environment. experience as a consultant/manager in access and/or pharmacoeconomics (desirable). ...
Join our team as a senior financial analyst to assist in the support of reporting and analytical needs of the combined iqvia™ organization. main functions: together with immediate supervisor assist in partnering with corporate function leaders with cost management: annual budget preparation, monthly forecast, monthly results review, ad hoc projects. assist in updating standardized monthly reports and perform analyses of financial results against budget / forecasts. assist during meetings with cost center managers to discuss forecast and preliminary budgets. highlight major concerns relating to forecasts or budget to immediate supervisor to seek guidance on how to proceed. assist in the development of functional operating review presentations. maintain detailed understanding of internal customer requirements and develop processes that will meet or exceed these requirements. requirements: bachelor’s degree in accounting and/or finance. three (3) to five (5) years of work experience in financial planning and analysis, including exposure to the monthly closing, budgeting & forecasting requirements of a publicly traded company. good analytical and financial modeling skills with the ability to quickly grasp and apply new concepts. ability to prioritize and coordinate multiple work requirements to meet deadlines. good oral and written communication skills. proficiency with hyperion (essbase) financial planning and reporting systems expertise with ms office tools, including good excel modeling skills experience with sap, and/or peoplesoft desirable. work experience within the pha...
Se regulatory affairs associate are you ready to shape the future of medicine? the race is on to speed up drug discovery and development to find answers for patients and their families. your skills could be critical in helping our teams accelerate progress. join our research and development team as regulatory affairs associate. mission statements: elaboration of dossier for lcm variations (cmc, labeling, admin) and renewals according to local requirements (all products categories, including biological and vaccines). elaboration of haq responses according to strategies defined by crm. elaborate and follow up dispatch plan in alignment with affiliate’s priorities and established deadlines according to process type. generate and propose to the regulatory affiliate regulatory submission strategies for the cmc variations received this position will suit an individual who is able to operate with discretion and confidentiality about sensitive data and with ability to prioritize among workloads and multiples sources of demands. main responsibilities: responsible for cp verification, dossier elaboration and dispatch of products from relevant bus to the countries in charge, ensuring compliance with local regulations and accomplishing timing needs. responsible for the dispatch plan of respective dossiers. focal point for communication with customers / interfaces (e.g.: rso and global cmc, operation, labelling, ivt etc) preparation of risk assessments of the dossiers before dispatch, including technical viability, when applicable. responsible for review of cp completeness and gathering...
Job overview provides high quality, on-time input to client projects in the health economics and outcomes research field. responsible for engaging local and regional clients to develop custom hta and other heor studies, developing innovative product offerings and leveraging latest innovation in technology and data science to develop value added solutions essential functions • under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions. health economic modeling • produce draft storyboards for simple health economic models and provide significant input to their further development • review literature to source the required inputs • produce support materials for completed economic models, e.g. reports and training programs market access strategy • collaborate in research projects and produce reports for projects delivering strategic advice to clients on research agendas, value proposition and market access outcomes research/health services research • under close supervision, performs quantitative or qualitative analyzes to assist in the identification of client issues and the development of client specific solutions. • assists in the design and structure of presentations that are appropriate to the characteristics or needs of the audience. • proactively develops a basic knowledge of consulting methodologies and the life sciences market through the delivery of consulting engagements and participation in formal and informal learning opportunities. • engagement based responsi...
As a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. as a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. we are seeking an experienced and highly motivated centralized study specialist i to join our team. this role involves managing clinical systems, supporting study documentation, ensuring compliance, and providing leadership and mentorship to junior team members. the successful candidate will play a pivotal role in the successful execution of clinical trials and contribute to process improvement initiatives. key responsibilities: clinical systems management: oversee and manage clinical systems.maintain study databases (ctms, iwrs, edc, etc.).support etmf management. study coordination: tr...
Job overview provides high quality, timely development and on-time input to solutions for heor studies, managed services, or implementation-oriented client projects. assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions. contributes to meeting client satisfaction objectives. essential functions • carry out work relating to the heor business areas (health economic modelling, market access strategy, value proposition) • work with supervision, indepently and/or as part of a project team on defined tasks • involve in business development/internal initiatives i.e. produce partial initial drafts of proposals based on client rfp and supporting information, participate in internal disseminations and make oral presentations to iqvia colleagues • project management/client liaison including client management tasks, attend client and other external meetings and presentations of own research/analysis • develop, review, implement and execution of prospective or retrospective outcome research protocols, statistical analysis plans and reports • carry out local data sourcing, search, collection and generation and produce support materials for completed economic models, develop analysis plan, input to the development/adaptation of complex health economic models • draft, revise, submit and present abstracts, posters and manuscripts for publication/ conference proceedings based on outcome research or economic models. assist in the submission process. qualifications • bachelor's degree required • degree in public health...
As a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. as a leading global contract research organization (cro) with a passion for scientific rigor and decades of clinical development experience, fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. with over 19,000 staff conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. we are seeking a dedicated sr centralized study associate to join our team. the successful candidate will be responsible for: clinical systems & access management: managing clinical systems and access.maintaining study databases (ctms, iwrs, edc, etc.).supporting the study team in data review and other related activities.tracking and following up with cras for outstanding issues.generating study-specific reports.managing internal/external communications.assisting in ensuring training compliance for study teams.managing study payments (site and vendor). data review: following up with cras...
Overview as a project manager, 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 comp...
As a project manager 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 o...
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