Job overview responsible for the on-time completion of heor & market access projects or components of large, complex projects for clients in the life sciences field. identifies and elevates potential new business opportunities and assists in the sale...
Description 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,...
We create best-in class products – from anti-aging serums, to immune support formulas, to online courses. our wellness formulas have been designed by one of america’s top anti-aging doctors, our products are fueling explosive growth. from the start, we’ve operated as a fully remote team, united by a shared mission, clear values, and a dynamic, high-performance culture. we move fast, play to win, learn from mistakes, and celebrate victories—together. many of our team members have been with us for over five years, consistently growing their skills, relationships, and impact along the way. we offer the perfect blend of stability, flexibility, and opportunity to shape your success. if you’re ready to be part of a supportive, highly-motivated team that’s breaking records and redefining what’s possible—apply now. company values: we’re a remote-first company, with an incredible, supportive culture. if you’re selected to join, here’s what you’re signing up for: we’re obsessed with what people respond to we’re scrappy we’re kaizen we follow through we give a damn we win and help win what's a protocol review specialist? a protocol review specialist is someone who attends a 20 minute protocol review appointment with a customer that has purchased a new health and wellness product. on the protocol review appointment, we walk a customer step by step through a carefully crafted health and wellness protocol designed to help them optimize their health with the product that they just purchased. about half of the time these customers could benefit from additional health an...
Job description aecom is looking for a construction coordinator for civil works for its offices in bogotá, colombia. responsibilities include, but are not limited to: providing technical leadership in a specialized area. applying extensive and diversified knowledge of engineering principles and practices in broad assignments and related fields. making independent decisions on technical problems and methods, and representing the organization at conferences. resolving significant issues, planning, and coordinating work. using advanced techniques, modifying and extending theories, principles, and practices in the field, related sciences, and disciplines. supervision and guidance largely pertain to overall objectives, critical issues, new concepts, and policy matters. receiving instructions in unusual conditions and developments. qualifications minimum requirements: bachelor's degree in civil engineeringor related disciplins + 8 years of experience or demonstrated equivalence of experience and/or education. general professional experience in civil works. additional information preferred skills and experience: professional degree in civil engineering or related fields, with postgraduate studies in specialization, master's, or doctorate. experience in directing or coordinating the construction or civil works of transportation infrastructure engineering projects, or the pmo for the construction of civil works for transportation infrastructure projects. availability to work in latin america. experience in having directed/coordinated construction contracts for civil works f...
Reasons could include the position has been filled or the company is not accepting new applicants. at blankfactor, we are dedicated to engineering impact. we are passionate about creating value by building best-in-class tech solutions for companies looking to transform, innovate, and scale. in every project, we aim to deliver work that moves the needle and drives measurable outcomes for our partners and clients. our full-stack development, data engineering, digital product, and enterprise ai solutions cater to a range of industries, including payments, banking, capital markets, and life sciences. we are headquartered in miami, florida, with offices in bulgaria, colombia, and romania, and are rapidly expanding our global footprint. our culture of engineering excellence, technical expertise, and care for both our clients and our talented workforce has made us one of the fastest-growing companies in america. we only hire the best and brightest. if you have talent and ambition, join us and be part of an environment that fosters innovation, collaboration, and growth. welcome to blankfactor! what you will do we are seeking a senior java engineer with extensive experience in java, jvm, and financial services to join our dynamic team. the ideal candidate has a background working at a big bank or faang company and excels in a fast-paced environment. as a senior java engineer at blankfactor, you will be a key contributor to the development and maintenance of our java-based applications. your expertise in java development, software architecture, and problem-solving will be instrumenta...
The integrated operations center optimization operator serves on the front-line of remote operations and is the primary contact for well operations support. utilizing remote surveillance programs, scada systems, and customized workflows, the operator can visualize problems from a unique perspective and quickly drive solutions. this position, based in eagle ford’s kenedy field office on a 7/7 rotation, will remotely perform system wide (from well to sales) surveillance, diagnostics & optimization in collaboration with field personnel. **_primary job responsibilities_**: communicate wells alarms to field staff; cygnet, intelligent, ghg, seismic identify immediate action alarms and perform shutdown if needed; communicate to field staff execute pcs curtailments when needed identify critical vs expected alarms during major downtime events; close interaction with mainline ioc controller collaborate with field operators with troubleshooting; communicate shutdowns and insights from trending/analysis manage trucking logistics and tank inventory; review and schedule load entries to meet marketing priorities, communicate priorities to carriers isolate wells producing to tanks during loading operations manage field requests to schedule transfer truck to work bottoms communicate to field staff hauling issues on location communicate with the field during emergency blackline calls; manage emergency dispatch if needed communicate mainline alarms to field staff; cf, cdp, oil delivery, ghg, dot remote pipeline surveillance / central facility troubleshooting; wells gassing out liquid lin...
**contribution & sponsorship specialist** - _ location_: bogotá, colombia_ - _ grade: _l2_ - _ hiring manager_: _florian baude_ - about the job_ - our hubs are a crucial part of how we innovate, improving performance across every sanofi department and providing a springboard for the amazing work we do. build a career and you can be part of transforming our business while helping to change millions of lives. ready? as_ co_ntribution & sponsorship specialist_ within our _global meetings & events_ team_, _you’ll_ _be r_esponsible for managing the end-to-end process for sponsorships & and charitable donations (contributions). the specialist will develop a strong understanding of the company designated systems supporting requests (e.g., gifts online, cybergrants, shift, aravo, cvent, coupa, sap, etc.) as well as the policies and procedures related to these areas._ **main responsibilities**: - report to the global lead and bring their experience and knowledge in the form of recommendations to meet sanofi’s purpose and goals, focusing on efficiency while always staying compliant at every level. - maintain centralized records for all sponsorship submissions & evidence of review & approvals. - support global business units with access, system issues, and necessary enhancements. - document payment information in the system and transfer of value where applicable. - point person for specified departments related to the sponsorship/contributions process. - the global events & engagement congress sponsorship specialist will be trained on the end-to-end event & engagement p...
Descripción de la publicación: **director of broking strategy - req **2527802 **bogotá, colombia** - would you like to join a diverse and inclusive team? are you looking to impact with your knowledge a leading transnational company? ¡ this opportunity is waiting for you! _ - this is a hybrid role with the flexibility to work both virtually and from our latam offices_ **aon is in the business of better decisions** at aon, we shape decisions for the better to protect and enrich the lives of people around the world. as an organization, we are united through trust as one inclusive, diverse team, and we are passionate about helping our colleagues and clients succeed. **what the day will look like** to be a technical facilitator for the commercial and customer service areas of the company, through the definition of the placement strategy for multi-line business (new new, new additional or renewal). - definition of the placement strategy: alignment with the customer service and commercial areas, on the coverage needs for our client's insurance programs and subsequent coordination with the placement team. - consolidation of information for quotes and market diagnosis: contact and negotiation with key insurance companies for the placement process of each of our clients. - quality control of quotations and offer construction: validation of compliance with the deliveries made by the technical managements in order to guarantee the commitments with our clients. - business monitoring and management reporting: ability to manage the data resulting from the placement proc...
**the opportunity**: at kin + carta, we’ve got opportunities to offer you — for growth, for leadership, for big, world-changing impact and for, dare we say it, fun. we are a global workforce that is committed to building a world that works better for everyone. and that starts with our kin. that’s why we’re proud of: - the life we create within our virtual walls, every day - our b corp certification - being great place to work certified in all eligible countries - the work we’ve done with some of the world’s most innovative companies **the role**: **kin + carta** is looking to hire a **senior spark data engineer **to join our growing team. if you are innovative, passionate about data and ai technologies, and look to continually learn and share your expertise, read on! **due to the sensitive nature of this client project, this role requires you to be onsite in our bogotá office 5 days a week.** **role responsibilities**: - demonstrate deep knowledge of the data engineering domain to build and support non-interactive (batch, distributed) & real-time, highly available data pipelines - build fault-tolerant, self-healing, adaptive, and highly accurate data computational pipelines - provide consultation and lead the implementation of complex programs - develop and maintain documentation relating to all assigned systems and projects - tune queries running over billions of rows of data running in a distributed query engine - perform root cause analysis to identify permanent resolutions to software or business process issues **minimum qualifications**: **we wan...
Growing mid-sized clinical research organisation (cro) , is seeking an ambitious business development director europe . this is a key opportunity for a proactive professional with a and a passion for developing strategic partnerships with biotech and pharma clients. role overview : the business development director will be responsible for establishing and expanding the company’s presence in european markets . the role will focus on early-phase clinical trials (phase 1-2) in oncology, cns, and rare diseases , working closely with biotech and pharmaceutical companies to drive business growth. from identifying high-potential opportunities to closing deals, this role plays a critical part in positioning the organisation as a leading partner in clinical research. key responsibilities : develop and execute a sales strategy to drive market expansion across europe. identify and engage with key biotech and pharma decision-makers to build long-term partnerships. manage rfps, lead negotiations, and deliver tailored solution presentations to potential clients. represent the company at industry conferences and networking events across europe. work closely with internal teams to align business strategies with market needs. ensure client satisfaction and ongoing relationship management to drive repeat business. requirements : proven experience in business development within a full-service cro, biotech, or pharma setting. strong understanding of early-phase clinical trials (phase 1-2), particularly in oncology, cns, and rare diseases. ability to develop new business...
**the opportunity**: at kin + carta, we’ve got opportunities to offer you — for growth, for leadership, for big, world-changing impact and for, dare we say it, fun. we are a global workforce that is committed to building a world that works better for everyone. and that starts with our kin. that’s why we’re proud of: - the life we create within our virtual walls, every day - our b corp certification - being great place to work certified in all eligible countries - the work we’ve done with some of the world’s most innovative companies **the role**: kin + carta is looking to hire a data analyst to join our growing capabilities team. if you are innovative, passionate about data and ai technologies, and look to continually learn and enjoy sharing expertise, read on! **due to the sensitive nature of this client project, this role requires you to be onsite in our bogotá office 5 days a week.** **role responsibilities**: - analyze a collection of raw data sets to create meaningful impact to large enterprise clients while maintaining a high degree of scientific rigor and discipline. - engineer data pipelines and products to help stakeholders make and execute data driven decisions. - communicate analytical findings in an intuitive and visually compelling way. - conducting deep dive analysis and designing kpis to help guide business decisions and measure success - engineering data infrastructure, software libraries, and apis supporting bi and ml data pipelines - architecting cloud data platform components enabling the above - building and tracking project timeline...
Descriptionat 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 on areas of medicine where we can make the biggest difference: cardiovascular & metabolism, immunology, infectious diseases & vaccines, neuroscience, oncology, and pulmonary hypertension. we are janssen. our patients inspire us. we collaborate with the world for the health of everyone in it. please visit https://www.janssen.com for more information. we are searching for the best talent for medical scientific liaison to be based in bogota, colombia. responsibilitiesbuild relationships with community and academic hcps focusing on changing behavior through the exchange of scientific knowledge. convey the value of the attributes related to the innovation (i.e., efficacy, safety, effectiveness, adherence, qol) to gain attribute endorsement with stakeholders. shape the market by changing behaviors within the hcp community during product pre-launching phases - prepare the market and medical community, accelerate adoption (pis engagement and pre-approval access programs). follow up on adoption, identifying barriers for behavior change for inline products. respond to scientific inquiries of hcps/investigators/healthcare systems and population health decision makers. integrate scientific data into real-life practice to meet customer/audience needs. identify...
Descriptionat 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 on areas of medicine where we can make the biggest difference: cardiovascular & metabolism, immunology, infectious diseases & vaccines, neuroscience, oncology, and pulmonary hypertension. we are janssen. our patients inspire us. we collaborate with the world for the health of everyone in it. please visit https://www.janssen.com for more information. we are searching for the best talent for medical scientific liaison to be based in bogota, colombia. responsibilitiesbuild relationships with community and academic hcps focusing on changing behavior through the exchange of scientific knowledge. convey the value of the attributes related to the innovation (i.e., efficacy, safety, effectiveness, adherence, qol) to gain attribute endorsement with stakeholders. shape the market by changing behaviors within the hcp community during product pre-launching phases - prepare the market and medical community, accelerate adoption (pis engagement and pre-approval access programs). follow up on adoption, identifying barriers for behavior change for inline products. respond to scientific inquiries of hcps/investigators/healthcare systems and population health decision makers. integrate scientific data into real-life practice to meet customer/audience needs. identify...
Description 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 on areas of medicine where we can make the biggest difference: cardiovascular & metabolism, immunology, infectious diseases & vaccines, neuroscience, oncology, and pulmonary hypertension. we are janssen. our patients inspire us. we collaborate with the world for the health of everyone in it. please visit https://www.janssen.com for more information. we are searching for the best talent for medical scientific liaison to be based in bogota, colombia. responsibilities 1. build relationships with community and academic hcps focusing on changing behavior through the exchange of scientific knowledge. 2. convey the value of the attributes related to the innovation (i.e., efficacy, safety, effectiveness, adherence, qol) to gain attribute endorsement with stakeholders. 3. shape the market by changing behaviors within the hcp community during product pre-launching phases - prepare the market and medical community, accelerate adoption (pis engagement and pre-approval access programs). 4. follow up on adoption, identifying barriers for behavior change for inline products. 5. respond to scientific inquiries of hcps/investigators/healthcare systems and population health decision makers. 6. integrate scientific data into real-life practice ...
Description 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 on areas of medicine where we can make the biggest difference: cardiovascular & metabolism, immunology, infectious diseases & vaccines, neuroscience, oncology, and pulmonary hypertension. we are janssen. our patients inspire us. we collaborate with the world for the health of everyone in it. please visit https://www.janssen.com for more information. we are searching for the best talent for medical scientific liaison to be based in bogota, colombia. responsibilities 1. build relationships with community and academic hcps focusing on changing behavior through the exchange of scientific knowledge. 2. convey the value of the attributes related to the innovation (i.e., efficacy, safety, effectiveness, adherence, qol) to gain attribute endorsement with stakeholders. 3. shape the market by changing behaviors within the hcp community during product pre-launching phases - prepare the market and medical community, accelerate adoption (pis engagement and pre-approval access programs). 4. follow up on adoption, identifying barriers for behavior change for inline products. 5. respond to scientific inquiries of hcps/investigators/healthcare systems and population health decision makers. 6. integrate scientific data into real-life practice ...
**who are we? **:**amaris consulting** is an independent technology consulting firm providing guidance and solutions to businesses. with more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade - this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries. our solutions focus on four different business lines: information system & digital, telecom, life sciences and engineering. we’re focused on building and nurturing a top talent community where all our team members can achieve their full potential. amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success. **brief call**: our process typically begins with a brief virtual/phone conversation to get to know you! the objective? learn about you, understand your motivations, and make sure we have the right job for you! **interviews** (the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). during the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. we will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. of course, you will also get to know amaris: our culture, our roots, our teams, and your career opportunities! **case study**: depending on the position, we may ask you to take a test. this could be a role play, a technical assessment, a problem-...
**who are we?**:**amaris consulting** is an independent technology consulting firm providing guidance and solutions to businesses. with more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade - this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries. our solutions focus on four different business lines: information system & digital, telecom, life sciences and engineering. we’re focused on building and nurturing a top talent community where all our team members can achieve their full potential. amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success. **brief call**: our process typically begins with a brief virtual/phone conversation to get to know you! the objective? learn about you, understand your motivations, and make sure we have the right job for you! **interviews** (the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). during the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. we will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. of course, you will also get to know amaris: our culture, our roots, our teams, and your career opportunities! **case study**: depending on the position, we may ask you to take a test. this could be a role play, a technical assessment, a problem-s...
Description 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 on areas of medicine where we can make the biggest difference: cardiovascular & metabolism, immunology, infectious diseases & vaccines, neuroscience, oncology, and pulmonary hypertension. we are janssen. our patients inspire us. we collaborate with the world for the health of everyone in it. please visit https://www.janssen.com for more information. we are searching for the best talent for medical scientific liaison to be based in bogota, colombia. responsibilities 1. build relationships with community and academic hcps focusing on changing behavior through the exchange of scientific knowledge. 2. convey the value of the attributes related to the innovation (i.e., efficacy, safety, effectiveness, adherence, qol) to gain attribute endorsement with stakeholders. 3. shape the market by changing behaviors within the hcp community during product pre-launching phases - prepare the market and medical community, accelerate adoption (pis engagement and pre-approval access programs). 4. follow up on adoption, identifying barriers for behavior change for inline products. 5. respond to scientific inquiries of hcps/investigators/healthcare systems and population health decision makers. 6. integrate scientific data into real-life practice ...
Who are we? amaris consulting is an independent technology consulting firm providing guidance and solutions to businesses. with more than 1000 clients across the globe, we have been rolling out solutions in major projects for over a decade - this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries. our solutions focus on four different business lines: information system & digital, telecom, life sciences and engineering. we’re focused on building and nurturing a top talent community where all our team members can achieve their full potential. amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success. **brief call**: our process typically begins with a brief virtual/phone conversation to get to know you! the objective? learn about you, understand your motivations, and make sure we have the right job for you! interviews (the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). during the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. we will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. of course, you will also get to know amaris: our culture, our roots, our teams, and your career opportunities! **case study**: depending on the position, we may ask you to take a test. this could be a role play, a technical assessment, a problem-solving scenario...
Growing mid-sized clinical research organisation (cro) , is seeking an ambitious business development director europe . this is a key opportunity for a proactive professional with a and a passion for developing strategic partnerships with biotech and pharma clients. role overview : the business development director will be responsible for establishing and expanding the company’s presence in european markets . the role will focus on early-phase clinical trials (phase 1-2) in oncology, cns, and rare diseases , working closely with biotech and pharmaceutical companies to drive business growth. from identifying high-potential opportunities to closing deals, this role plays a critical part in positioning the organisation as a leading partner in clinical research. key responsibilities : develop and execute a sales strategy to drive market expansion across europe. identify and engage with key biotech and pharma decision-makers to build long-term partnerships. manage rfps, lead negotiations, and deliver tailored solution presentations to potential clients. represent the company at industry conferences and networking events across europe. work closely with internal teams to align business strategies with market needs. ensure client satisfaction and ongoing relationship management to drive repeat business. requirements : proven experience in business development within a full-service cro, biotech, or pharma setting. strong understanding of early-phase clinical trials (phase 1-2), particularly in oncology, cns, and rare diseases. ability to develop new business pip...
Job description as part of amaris growth, we are looking for a new talent within our finance team. you will join the corporate finance & treasury department, being part of a multicultural team with people based in canada, france, spain, south africa, singapore. we are recruiting a cash manager to support the growing activity on the american (latam & north america) perimeter. reporting to the head of treasury & financing, you will play a major role in the administrative and financial department, and you will be responsible for the following tasks: **cash management**: manage daily treasury operations on our treasury management system (kyriba) and with banks in canada, usa, mexico, chile, brazil & colombia implement banking connectivity in latam with swiftnet fileact protocol optimize & automate cash forecast & fx monitoring tools monitor & analyze bank charges provide recommendations on new innovative solutions to implement from banks or fintechs **financing & debt management**: negotiate bank credit lines, real estate financing lines & other type of loans with our financial partners for local investments **investment solutions**: deploy and oversee local corporate cash investment strategies and operations develop and manage local processes for daily inhouse investments for short-term liquidity recommend and implement updates to investment guidelines **your profile**: bachelor’s degree in finance at least 2 years of experience in a corporate treasury department or in a banking role strong interest in cash, financing and investment topics with entrepreneurial...
**your next step is at rappi!** rappi is one of the first latin american unicorns and a start-up that continues to focus on growing and making life easier for our users. as a company, we seek to continue improving the services we already offer, add more to our offer and continue expanding throughout the latin american continent.**role objective**: - develop, implement, and maintain a system of quality and reliability testing for the team products and development processes. **main responsibilities**: - testing and sampling products, ensuring they meet set standards and specifications. - developing quality control policies and standards for the team to follow. - training team members on the quality control processes and policies. - overseeing quality control processes of the team. - conducting audits of product inventory and documentation. **key requirements**: - bachelor in computer sciences or related fields. - strong analytical and problem-solving skills. - strong supervisory and leadership skills. **desired requirements**: - experience designing qa guidelines and specifications for a team to follow. - experience testing complex systems. - experience testing micro-service architectures. he leído y acepto la autorización de datos personales de rappi s.a.s- - conforme a la política de tratamiento de datos personales i have read and accept the authorization of personal data from rappi s.a.s- - in accordance with the personal data treatment policy...
Job description as a key account specialist at amaris consulting, you will be point of contact for all financial and administrative tasks relating to our clients’ accounts. detailed responsibilities **customer billing management**: collect and verify billing information from multiple internal sources. generate accurate and detailed invoices using our erp system. ensure all invoices comply with legal and tax requirements. manage billing discrepancies **vendor invoice processing**: receive and process vendor invoices related to specific projects. verify invoice accuracy against purchase orders and contracts. request vendor payments according to agreed terms **project tracking and reporting**: maintain up-to-date records of each project's financial status. generate monthly reports on billing progress by project. collaborate with controlling department to resolve financial discrepancies. **monthly closing and reporting**: prepare and reconcile accounts for monthly closing. generate detailed financial reports for management review. assist in preparing presentations for monthly closing meetings. analyze trends and propose improvements in billing processes. **data and systems management**: maintain accurate customer databases. continuously update and improve billing processes in the erp system. ensure the integrity and confidentiality of financial data. propose and implement improvements to billing systems. **interdepartmental collaboration**: work closely with the sales team to ensure timely billing. coordinate with the legal department to ensure contr...
**company description** yuxi global (powered by veritas automata) has been a leading force in empowering life sciences companies to achieve their digital goals since 2005. having partnered with nearly 300 clients, yuxi global has played a crucial role in advancing digital solutions for companies in life sciences. utilizing cutting-edge technologies such as microsoft azure, powerbi,.net custom development, node.js, react, and ux/ui design, we deliver impactful solutions that drive business growth and captivate audiences. we are looking for a skilled bi developer to support our reporting initiative, which is focused on delivering accurate, audit-ready reports through the enterprise reporting and analytics (era) platform. **key responsibilities**: - develop, maintain, and optimize looker dashboards and visualizations for hca compliance reporting. - build and extend lookml models to support business requirements and ensure data accuracy. - translate business and regulatory requirements into technical specifications and reporting logic. - perform source-to-target mapping and work closely with data architects to ensure proper model alignment. - query and validate data in snowflake using sql for use in looker reports. - collaborate with data analysts, qa, and product owners to ensure reporting quality, accuracy, and usability. - ensure all reports meet audit, regulatory (e.g., hca), and performance standards. **qualifications** required qualifications**: - 4+ years of experience in **bi/reporting** development - strong proficiency in **looker and lookml modelin...
**lv purchasing specialist** **work location: colombia** **about rws**: rws holdings plc is the world’s leading provider of technology-enabled language, content management and intellectual property services. we help our customers to connect with and bring new ideas to people globally by communicating business critical content at scale and enabling the protection and realization of their innovations. our vision is to help organizations interact effectively with people anywhere in the world by solving their language, content and market access challenges through our collective global intelligence, deep expertise and smart technology. customers include 90 of the globe’s top 100 brands, the top 10 pharmaceutical companies and 18 of the top 20 patent filers worldwide. our client base spans europe, asia pacific, and north and south america across the technology, pharmaceutical, medical, legal, chemical, automotive, government and telecommunications sectors, which we serve from offices across five continents. founded in 1958, rws is headquartered in the uk and publicly listed on aim, the london stock exchange regulated market (rws.l). **rws regulated industries division**: provides a full suite of language services exclusively for highly regulated industries such as life sciences, healthcare, financial services, and legal industries. this includes language solutions for clinical trial management and linguistic validation of clinical outcomes assessments (coas), insurance, retail, commercial and investment banking, compliance, mergers & acquisitions, and litigation. *...
**your next step is at rappi!** rappi is one of the first latin american unicorns and a start-up that continues to focus on growing and making life easier for our users. as a company, we seek to continue improving the services we already offer, add more to our offer and continue expanding throughout the latin american continent.**role objective**: - develop, implement, and maintain a system of quality and reliability testing for the team products and development processes. **main responsibilities**: - testing and sampling products, ensuring they meet set standards and specifications. - developing quality control policies and standards for the team to follow. - training team members on the quality control processes and policies. - overseeing quality control processes of the team. - conducting audits of product inventory and documentation. **key requirements**: - bachelor in computer sciences or related fields. - strong analytical and problem-solving skills. - strong supervisory and leadership skills. **desired requirements**: - experience designing qa guidelines and specifications for a team to follow. - experience testing complex systems. - experience testing micro-service architectures. he leído y acepto la autorización de datos personales de rappi s.a.s- - conforme a la política de tratamiento de datos personales i have read and accept the authorization of personal data from rappi s.a.s- - in accordance with the personal data treatment policy...
Tasks responsible for developing, reviewing, finalizing, and maintaining clinical trial documents such as informed consent forms. apply knowledge of gcp guidelines, regulatory requirements, privacy standards, biological samples standards, therapeutic areas, and investigational medicinal products (imps) to review and develop informed consent forms (icf). ensure that the content of the master informed consent form aligns with the protocol and fully informs potential research subjects about the study to aid their decision-making. guarantee that the consent forms are understandable, using clear language accessible to participants, including scientific and medical terminology. write and edit documents in compliance with global industry standards. incorporate client-specific guidance and requirements into the master informed consent form during development and review. support the development, review, and approval of master templates to facilitate protocol and site activation. create, review, and revise training materials and plans to meet team training needs. communicate timely and appropriately with all stakeholders regarding project status, issues, or safety concerns. liaise with project managers or designees to report trends, outstanding issues, or safety concerns that could impact trial delivery or patient safety. skills strong knowledge of the drug development process. good understanding of fda ind/nda requirements. comprehensive understanding of regulations related to clinical trials, including fda regulations, biological samples, gdpr, and gcp guidelines. kn...
Middle fullstack developer. net & angular (sql focus) company description yuxi global (powered by veritas automata) has been a leading force in empowering life sciences companies to achieve their digital goals since 2005. we specialize in providing c...
Mid full stack developer (angular. net & python) full-time yuxi global (powered by veritas automata) has been a leading force in empowering life sciences companies to achieve their digital goals since 2005. we specialize in providing comprehensive so...
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