For project management services. what makes you a fit: the technical part: bachelor of science in engineering (mechanical or electrical) and at least five (5) years of experience in project management within the pharmaceutical industry. shift: admini...
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Icon plc is a world-leading healthcare intelligence and clinical research organization. from molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. with our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. our people are our greatest strength, are at the core of our culture, and the driving force behind our success. icon people have a mission to succeed and a passion that ensures what we do, we do well. we have an incredible opportunity for a **clinical data lead** to join the team. **location**: - mexico (home based - colombia (home based) **overview of the role**: as a clinical data lead (cdl) you will be the point of contact for day to day activity on a study with key responsibilities for study set-up and close-out tasks as well as overseeing and coordinating tasks delegated to the study team members both locally and in other offices. you will also coordinate with data management teams, studies and programs of studies and independently oversee the performance of data management activities on multiple studies. - independently prepare all materials and take part in study kick off (internal and external) meeting. - review all activity on an ongoing basis to identify out of scope tasks and bring to the attention of the dmpm and contract analyst. - lead the development of specifications, implementation, and testing for the ecrf or paper crf. ...
As a clinical research associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. a cra is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. you will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed. - may serve as preceptor, providing training to less experienced clinical team members. - may ...
Under the leadership and directional guidance of the associate director, external audits & inspections management lead, who drives and supports the development and implementation of strategies and initiatives to prepare organon research & development the associate director will support activities related to inspections and external audits for the various b&o; functions related gxps and will partner with cross-functional leads and subject matter experts (smes) to ensure an advanced understanding of health authority perspective and expectations and can help those colleagues understand this mindset. ***this role can be 100% remote in the north america/latam** **responsibilities** - execute the inspection and external audit strategy, facilitating and supporting on-site and remote audits and health authority inspections. inspection experience a plus. - support the global audit and inspection readiness program. - contribute on the development of standard policies and procedures and supporting tools to enable flawless execution in all external audits and inspections. - collaborate with cross-functional teams to ensure all capa commitments related to external audits or inspections are completed on time and determined to be effective. - provide support in establishing and maintaining a compliance governance structure, providing metrics review of key quality & compliance activities. - prioritize and ensure ad hoc and emerging topics are reviewed and escalated in a timely manner. - ensure organon responses to any external audit or inspection report are concise and strateg...
At johnson & johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity. diversity & inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. regardless of your race, belief, sexual orientation, religion, or any other trait, you are welcome in all open positions at the largest healthcare company in the world. when you join johnson & johnson, your move could mean our next breakthrough. this is a cross-sector role. learn more about our sectors: **medical devices** at johnson & johnson medical devices companies, we are using our breadth, scale, and experience to reimagine the way healthcare is delivered and to help people live longer, healthier lives. in a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics, and interventional solutions with the big ideas of others to design and deliver doctor and patient-centric products and solutions. we are in this for life. we are changing the trajectory of human health, you can too. **pharmaceuticals** at janssen, we’re creating a future where disease is a thing of the past. we’re the pharmaceutical companies of johnson & johnson, working tirelessly to make that future a reality for patients everywhere by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart. we focus...
Prestar un servicio de calidad y de apoyo a los clientes externos e internos para reducir las quejas y reclamos. - indagar la solicitud del requerimiento del cliente y dar respuesta inmediata y eficiente de acuerdo al alcance, apoyado en los procesos relacionados. - realizar proceso de corte en sap y solicitar a logística bodega entrega de material para el proceso de adecuación, etiquetado y entrega al cliente. - solicitar tiquetes aéreos y reservas de hotel de acuerdo a itinerario informado; se confirma por medio de correo al asesor comercial. - envío de documentos a gerencia y financiero para realizar análisis financiero y confirmar aprobación de crédito. - solicitud, recepción, validación y archivo de los documentos enviados por los clientes para creación, actualización y reactivación. - seguimiento a liquidaciones, ingresos de material a sap y solicitud de precios para facturar. - instrucción y seguimiento de registros de importación, ica, invima o productos controlados - recepción, revisión, digitalización y entrega al cliente de facturas de importación, exportación, re expedición junto con los demás documentos para los procesos de nacionalización del cliente. - trazabilidad de arribo a bodega de cargas aéreas y marítimas - envío al cliente los documentos de transporte junto con los datos de reserva (sea/ air) para aprobación de despacho previa obtención de los permisos de importación. - atender requerimientos de ventas tipo de puesto: tiempo completo, indefinido salario: $1.300.000 - $1.400.000 al mes consideraciones ante el covid-19: trabajo en casa,...
**company description**: are you ready to accelerate your career? join cielo as a recruiter! a career at cielo will give you the opportunity to work with the industry’s smartest people and to take ownership of your success! cielo is a brand that reflects our big idea - that talent is rising - and with it our opportunity to rise above. we create careers for ambitious people by moving beyond traditional assumptions of what it means to work in talent acquisition. cielo is the world's leading talent acquisition partner. we deliver a better talent experience for everyone through talent acquisition, search, consulting, and digital accelerators. with our fresh approach - we design and build comprehensive, proven solutions inspired by technology to find and keep the unique talent that elevates our clients above the competition. **work arrangemente**:remote **language requirements**:fluent in english and spanish **specific needs**:recruitment experience in the pharmaceutical sector **responsibilities**: - solicit and pursue referrals from business networks and/or internal referrals. - issue skills testing as needed and evaluate results (if process dictates). - review background and reference information (if process dictates). - partner with hiring leader to determine offer details, using market data and compensation guidelines to support recommendations. - service excellence: - strict adherence to all regulations (ofccp and all other compliance standards set forth). - provide accurate and regular reporting of recruiting activities to the hiring leader and cielo l...
Caring for the world, one person at a time has inspired and united the people of johnson & johnson for over 125 years. we embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. with $82.1 billion in 2020 sales, johnson & johnson is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices markets. employees of the johnson & johnson family of companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. if you have the talent and desire to touch the world, johnson & johnson has the career opportunities to help make it happen. thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. proud to be an equal opportunity employer. johnson & johnson is the world's most comprehensive and broadly-based healthcare company, touching the lives of nearly a billion people every day. our family of companies throughout the world compete in consumer, pharmaceutical and medical devices & diagnostics markets and have the skills and resources to tackle the world's most pressing health issues. - _ nchc is recruiting for a gs strategy director with their global services organization global services is the global shared services organization supporting multifunctional services delivery. they perform select functional work in a consistent manner across regions using simplified, standa...
As clinical research associate (cra), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. a cra is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. you will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed. - may serve as preceptor, providing training to less experienced clinical team members. -...
Caring for the world, one person at a time has inspired and united the people of johnson & johnson for over 125 years. we embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. with $82.1 billion in 2020 sales, johnson & johnson is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices markets. employees of the johnson & johnson family of companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. if you have the talent and desire to touch the world, johnson & johnson has the career opportunities to help make it happen. thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. proud to be an equal opportunity employer. johnson & johnson is the world's most comprehensive and broadly-based healthcare company, touching the lives of nearly a billion people every day. our family of companies throughout the world compete in consumer, pharmaceutical and medical devices & diagnostics markets and have the skills and resources to tackle the world's most pressing health issues. - _ nchc is recruiting for a gs strategy director with their global services organization global services is the global shared services organization supporting multifunctional services delivery. they perform select functional work in a consistent manner across regions using simplified, standa...
**job description**: our clinical research and pharmacovigilance team push the boundaries of global healthcare through research and innovation. through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. **position overview**: under the direction of the applicable management, the clinical data manager is responsible for executing end to end data management activities pertaining to clinical trials, including but not limited to; data management tool and system development, validation and maintenance, data collection, data integrity review and reconciliation, query management, medical coding, and database lock preparation, in compliance with our company standard operating procedures and guidelines. **primary activities include, but are not limited to**: - receives the study related paper documents from sites or other functional areas, and transfers to data entered for processing. - performs sponsor data entry as applicable per data management plans following entry guidelines. - participates in the development and change request implementation of data management tools and systems for the clinical trial data management activities - execute data validation activities in accordance with relevant standard operating procedures. - raises questions to investigational site staff and internal and external vendors, reviews responses and corresponding data corrections to confirm identified issue resolution. - responsible for the execution of user acceptance testing of data m...
As a senior regulatory affairs specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. the senior regulatory affairs associate has responsibility for providing comprehensive regulatory services to clients within the pharmaceutical, biologic, medical device or other regulatory services environments. this will include support for assessment, registration, maintenance and other activities as assigned. you will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. working in this program you will feel challenged and supported to advance in your professional career while making a truly impact. **what you will be doing**: the regulatory affairs specialist will be working with drugs' registration according to the local regulatory agencies. - perform all electronic submissions of registration and post-registration requests to regulatory agencies. - ensure all expected/required correct data is updated/ uploaded in the systems (veeva) - supports assigned teams in the preparation of all submission types in adherence with applicable legislation, regulations and guidelines facilitating approvals and continued client compliance. - maintains a positive and productive liaison with internal and external contacts. this may include clients, regulatory agencies, and related institutions. - assists in the development of assessments and strategic regulatory plans for client product development programs. supports the develo...
As a clinical research associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed. - may serve as preceptor, providing training to less experienced clinical team members. - may be assigned clinical tasks where advanced negotiating skills are required. **you are**: - bachelor’s degree in a health, life sciences or other relevant field of study. ...
Management assistant - colombia, bogota hybrid: office/remote icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development management assistant office based role (hybrid) - mexico city, mexico - bogotá, colombia icon plc is a world-leading healthcare intelligence and clinical research organisation. from molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. with our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. our people are our greatest strength, are at the core of our culture, and the driving force behind our success. icon people have a mission to succeed and a passion that ensures what we do, we do well. the role: as a management assistant at icon, your job is essential in latam regional support across all divisions (ibt, ipd, iod, idc), supporting the regional leadership governance meetings and actions, capabilities & country input for sales/pm/feasibility/ssu, etc. this is a role that responds to the special requirement and needs for the region to have a governance and oversight that helps the global services be able to receive information on latam and respond to growth in the region for clinical operations this support includes quality...
As a clinical research associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed. - may serve as preceptor, providing training to less experienced clinical team members. - may be assigned clinical tasks where advanced negotiating skills are required. **you are**: - bachelor’s degree in a health, life sciences or other relevant field of study. ...
Compañía comercializadora de insumos y material de empaque para el sector farmacéutico requiere un tecnólogo en comercio exterior o carreras a fines de negocios internacionales, con experiência de uno a dos años, recién egresado con ganas de aprender, persona proactiva, analítica y buena actitud de servicio, con nível de ingles medio, escrito, para apoyo al proceso de compras. tipo de puesto: tiempo completo salario: $1.300.000 - $1.500.000 al mes consideraciones ante el covid-19: medidas básicas de limpieza y desinfección, uso tapabocas opcional, trabajo en casa...
Compañía comercializadora de insumos y material de empaque para el sector farmacéutico requiere un tecnólogo en comercio exterior o carreras a fines de negocios internacionales, con experiência de uno a dos años, recién egresado con ganas de aprender, persona proactiva, analítica y buena actitud de servicio, con nível de ingles medio, escrito, para apoyo al proceso de compras. tipo de puesto: tiempo completo salario: $1.300.000 - $1.500.000 al mes consideraciones ante el covid-19: medidas básicas de limpieza y desinfección, uso tapabocas opcional, trabajo en casa...
Site management associate i psi cro ag bogota, d.c., capital district, colombia join our international team as a site management associate i, supporting clinical research projects by streamlining communication, maintaining systems, and managing documents and information. responsibilities include: - acting as the main contact between site personnel and cras, assisting with queries and edc completion. - serving as the primary contact for vendors, study supplies, and access management. - ensuring pre-study testing of local site facilities is completed. - assisting monitors with documentation in ctms and tracking site issues and actions. - managing clinical supplies' order, receipt, storage, distribution, return, and reconciliation. - handling regulatory submissions and notifications, staying updated on local regulations. - coordinating audits and inspections. - managing the tmf at site and country levels, including document filing and updates. - organizing and tracking training for site teams on vendor systems. - reviewing study documentation and translation statuses. - ensuring proper safety information flow with investigative sites. qualifications: - degree in life sciences. - experience in administrative roles, preferably internationally. - experience as a cta in cros and in clinical research. - knowledge of local regulations. - proficiency in english and spanish. - skillful in ms office. - ability to work dynamically in a team and communicate effectively. additional information: advance your career in clinical research by coordinating tasks and growing with the com...
Join amgen's mission of serving patients at amgen, if you feel like you're part of something bigger, it's because you are. our shared mission—to serve patients living with serious illnesses—drives all that we do. since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. with our focus on four therapeutic areas –oncology, inflammation, general medicine, and rare disease– we reach millions of patients each year. as a member of the amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. our award-winning culture is collaborative, innovative, and science based. if you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the amgen team. join us and transform the lives of patients while transforming your career. commercial pricing manager (bogotá) what you will do let's do this. let's change the world. in this vital role you will a strategic and results-driven pricing manager to join our team in colombia, focusing on the pharmaceutical and biotechnology sectors. this critical role will be responsible for designing, implementing, and monitoring pricing strategies that align with business objectives, ensure regulatory compliance, and strengthen our competitive position in the market. the pricing manager will collaborate with cross-functional teams to drive profitability and optimize pricing models for innovative therapies and pharmaceutical products: - prici...
Job overview 50% of the role is to ensure overall client satisfaction as prerequisite for further successful business development and 50% of the role is to secure and grow our base business revenue. essential functions • under direct guidance, coordinates iqvia sales, consulting, service and business line activity to ensure that client needs are met following an account plan to achieve iqvia budget and client satisfaction targets. • client service - represents iqvia to the client and the client to iqvia in all service and sales related activity - manages basic accounts (approximately 2 to 3) - builds client relationships across the client organization, including business insiders - resolves 1st line service issues, and coordinates 2nd line support issues with the service teams - ensures thorough service reviews and transaction surveys that service agreements, contract specifications, and product deliverables meet clients’ specifications, including timeliness and quality • sales - secures renewal contracts - establishes a tactical and strategic understanding of the client’s business issues, and assists with developing a compelling solution using appropriate iqvia products and services - assists with the coordination of business development and service activity with the account director, sales, consulting and service specialists to validate opportunities to achieve account plan, revenue and client satisfaction targets - assists with the development of strategy for expanding scope of existing contracts and identifying new business and win back opportunities qualification...
**senior sales representative** **villavicencio, meta** **competitive salary & excellent benefits package** - working with customers in the medical and pharmaceutical fields, you’ll take ownership for your own area of the business. managing your own territory, you’ll design and implement medical marketing strategies. you’ll build trust and relationships. you’ll educate doctors, medical and pharmaceutical specialists to understand the benefits of our products. ultimately helping to improve the lives of millions of patients.**you’ll succeed because** - you know what’s needed to be successful in clinical sales. you understand medical research and trials process. clinical specialists have confidence in you because you understand their relevant disease areas and how different products act. you’re articulate and professional, you build long lasting relationships based on trust. you’re independent and entrepreneurial. just like us.**you’ll love it because** - you’ll get to make an impact like never before. you’ll be responsible for your own projects - we can’t wait to listen to your ideas. the products you get out there will make people’s lives better. our iconic brands will provide an incredible platform for you. and our dynamic, ownership-driven culture will help bring the very best out of you, every day.**equality**: at reckitt, we recognise that in real life, great people don’t always ‘tick all the boxes’. that’s why we hire for potential as well as experience. even if you don’t meet every point on the job description, if this role and our company feels like a good fit...
Diversity, equity & inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. regardless of your race, belief, sexual orientation, religion, or any other trait, you are welcome in all open positions at the largest healthcare company in the world. when you join johnson & johnson, your move could mean our next breakthrough. johnson & johnson is recruiting for a finance business partner, located in bogotá/colombia. key responsibilities: - provides recommendations to business partners. analyzes financial reports and related analyses. - audits the financial planning process and reviews the use of financial models. - performs highly complex financial analysis and research. - monitors department expenses and capital budgeting through tracking and reporting activities. - presents complex analysis to management. - establishes analysis and delivers insights that link financial data to organizational strategies. - forecasts budgetary successes based upon market data and historical trends. - audits monthly closing. **qualifications**: **qualifications**: **education**: bachelor’s degree in finance, business administration, economics, or a related field experience and skills: required: - at least 4-5 years of professional experience in financial controlling, fp&a;, finance business partner or related fields. - good problem-solving and analytical skills. - medium/ high english level. preferred: - mayor in finance ...
**consultant**: job description and tasks **consultant responsibilities**: the digital consumer insights analyst consultant is responsible for duties including but not limited to the following: - identifying and contextualizing both macro and micro trends relevant to atcs’ clients; trends to be identified through own research (keeping up-to-date on relevant news sources), plan and analyze primary research based on digital sources and synthesizing secondary research sources. - with trends in mind, identifying strategic opportunities and making well thought out recommendations to inform our clients’ business decisions. - acting as a liaison between the atcs and the client through relationship building, proactively anticipating consumer research needs and representing the ‘voice of the consumer’ during meetings and presentations. - serving as a trusted advisor to brand and/or consumer insights teams when questions regarding the consumer arise. - conducting qualitative research projects based primarily on social media and digital data to answer questions in multiple areas including product development, brand strategy, communication, tracking, and positioning for our clients’ brands. - reporting and presenting insightful findings with actionable recommendations to key partners **requirements** - 7-10 years of experience in qualitative research or similar field. - fluent spanish required; some knowledge of portuguese is desired. - prior knowledge of qualitative research methodologies is required. - strong analytical thinking and writing skills are required in bot...
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. conducting operations in more than 90 countries, fortrea is transforming drug and device development for partners and patients across the globe. fortrea is proud to be an equal opportunity employer: as an eoe/aa employer, fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. we make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. we encourage all to apply. for more information about how we collect and store your personal data, please see our privacy statement ....
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. **did you know?** **job summary**: the in-house clinical research associate (ihcra i) is an essential member of a clinical project team responsible for the execution of a clinical research project. the degree of responsibility given to the ihcra i shall reflect their experience, and level of contribution which they can make to the project. the work will involve clinical operations activities which will be conducted in an office or home based setting for designated projects as well as some travel to conduct site visits or to attend client or internal team meetings as needed. the ihcra i will be responsible for assisting with ensuring quality and integrity of data, and additional study related activities to support the efforts of study team members. activities will be conducted in compliance with company or sponsor sop, regulatory standards and applicable guidelines **experience** minimum required: - at least one year of experience in a related field, (e.g. medical, clinical, pharmaceutical, laboratory research, data analysis, data management or technical writing). one ye...
**company description** are you ready to accelerate your career? join cielo as a recruiter! a career at cielo will give you the opportunity to work with the industry’s smartest people and to take ownership of your success! cielo is a brand that reflects our big idea - that talent is rising - and with it our opportunity to rise above. we create careers for ambitious people by moving beyond traditional assumptions of what it means to work in talent acquisition. cielo is the world's leading talent acquisition partner. we deliver a better talent experience for everyone through talent acquisition, search, consulting, and digital accelerators. with our fresh approach - we design and build comprehensive, proven solutions inspired by technology to find and keep the unique talent that elevates our clients above the competition. **work arrangemente**:remote **language requirements**:fluent in english and spanish **specific needs**:recruitment experience in the pharmaceutical sector **responsibilities**: - solicit and pursue referrals from business networks and/or internal referrals. - issue skills testing as needed and evaluate results (if process dictates). - review background and reference information (if process dictates). - partner with hiring leader to determine offer details, using market data and compensation guidelines to support recommendations. - service excellence: - strict adherence to all regulations (ofccp and all other compliance standards set forth). - provide accurate and regular reporting of recruiting activities to the hiring leader and cielo le...
Principal biostatistician | clinical | pharma (fsp) top global pharma (fsp) via global cro fully remote fte who will you be working with? you'll be dedicated to a global pharmaceutical powerhouse driven by science, powered by data, and inspired by a ...
Home based icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of c...
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