Join to apply for the netsuite data architect role at agentic dream 2 days ago be among the first 25 applicants join to apply for the netsuite data architect role at agentic dream direct message the job poster from agentic dream skilled project manag...
Senior data analyst bogota, colombia. only cvs submitted in english will be considered. the opportunity: anthology delivers education and technology solutions so that students can reach their full potential and learning institutions thrive. our missi...
Our mission swapcard is the leading ai-powered event platform designed to drive revenue growth and foster meaningful connections at in-person and hybrid events. we recognize the importance of teamwork in successful events; that's why swapcard is fueled by a team of innovators who are passionate about helping organizers build future-proof events. our vision at swapcard, we believe in the power of meaningful connections. this belief fuels our commitment to pioneering modern solutions that empower organizers to create engaging event experiences. guided by our commitment to excellence and collaboration, we aim to redefine the landscape of event technology, setting new standards for engagement, accessibility, and impact. our beliefs at swapcard, diversity is at the core of our success. with 42 nationalities represented among our 180+ team members, we champion diversity as a catalyst for creativity, collaboration, and unparalleled innovation. we believe that by embracing a multitude of backgrounds, cultures, and viewpoints, we can truly understand and cater to the needs of our global community of event organizers and participants. our full remote opportunities empower our team to thrive, no matter where they are in the world, fostering a culture of flexibility and inclusion. the role we’re looking for a backend engineer to join one of our squads dedicated to building and enhancing the core systems that drive swapcard’s capabilities. you’ll play a key role in designing, developing, and delivering high-quality, scalable solutions for event organizer; while collabora...
**job title**: regional stability monitoring specialist - location: bogota - % of travel expected: as per business needs - job type: permanent **about the job** **our team**: sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. from prevention to treatment, sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions. the global m&s; services acts as a cornerstone to this effort. our team is responsible for delivering and supporting global m&s; teams by acting as a crucial link between our r&d; and manufacturing facilities, playing a vital role in securing the present portfolio and delivering future launches of high-quality and innovative drugs and vaccines. **main responsibilities**: - prepare data for analysis by using suitable statistical tools - provide training on good documentation practices and associated rules that must be applied when managing reports for stability management about you - ** experience**: experience in pharmaceutical (human or animal), quality control, quality assurance operation, product development (i&d;, formulation), process/analytical validations. - ** soft skills**: proficient in problem-solving, attention to detail, and good organizational skills. ability to work collaboratively with cross-functional teams in a flexible and proactive manner. strong analytical skills. agile thinker and l...
**job title**: regional stability monitoring specialist - location: bogota - % of travel expected: as per business needs - job type: permanent **about the job** **our team**: sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. from prevention to treatment, sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions. the global m&s; services acts as a cornerstone to this effort. our team is responsible for delivering and supporting global m&s; teams by acting as a crucial link between our r&d; and manufacturing facilities, playing a vital role in securing the present portfolio and delivering future launches of high-quality and innovative drugs and vaccines. **main responsibilities**: - prepare data for analysis by using suitable statistical tools - provide training on good documentation practices and associated rules that must be applied when managing reports for stability management about you - ** experience**: 2-4 years of experience in pharmaceutical (human or animal), quality control, quality assurance operation, product development (i&d;, formulation), process/analytical validations. - ** soft skills**: proficient in problem-solving, attention to detail, and good organizational skills. ability to work collaboratively with cross-functional teams in a flexible and proactive manner. strong analytical skills. agile ...
Location: latam, remote position type: temporary contract until dec/2025 (+ possibility of extension) position summary data meaning is a front-runner in business intelligence and data analytics consulting, renowned for our high-quality consulting services throughout the us and latam. our expertise lies in delivering tailored solutions in business intelligence, data warehousing, and project management. our strength lies in our global team of 95+ consultants, all working remotely, embodying a collaborative, inclusive, and innovation-driven work culture. we are seeking an experienced power bi & snowflake administrator to manage and maintain both platforms for one of our customers. the ideal candidate will ensure optimal performance, stability, security, and scalability of these environments. this role involves installation, configuration, monitoring, troubleshooting, user support, and adherence to industry best practices. key responsibilities power bi administration - administer and maintain power bi service, power bi report server, and related environments. - perform installation, configuration, and upgrades of power bi components. - monitor system performance, troubleshoot issues, and optimize dashboards/reports for efficiency. - manage power bi workspaces, user roles, permissions, and authentication settings. - implement and enforce best practices for report development, scheduling, and execution. - provide technical support to end users, ensuring seamless report execution. - collaborate with it teams to integrate power bi with enterprise systems such as data...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
Survey delivery & innovation associate (bogota) dialectica bogota, d.c., capital district, colombia survey delivery & innovation associate (bogota) dialectica bogota, d.c., capital district, colombia 2 days ago be among the first 25 applicants dialectica is a leading b2b information services firm that serves the world's top consulting, investment and largest corporate businesses, by enabling them to gather real-time information and insights from industry experts across various markets, industries, and regions. driven by our mission to achieve unparalleled customer recognition, we are developing the most trusted and innovative knowledge-sharing platform in the world. dialectica has been recognized as one of europe's fastest-growing companies by the financial times for 5 years in a row, a top employer for recent graduates by the career directory in canada and a best workplace. we believe in supporting our people to do their best work and grow, and building a dynamic, empowering, and respectful workplace is core to our purpose: accelerate the shift to a prosperous society by empowering better decision-making. about the role as an associate within the survey delivery & innovation team, your role is to partner with our clients to understand their quantitative b2b insights needs and to translate their requirements into best-in-class surveys - advising them on asking the right questions; programming the survey from scratch, conducting quality control on survey responses, visualizing the outputs and providing key results takeaways. we're looking for passionate candidat...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
Get ai-powered advice on this job and more exclusive features. niche is the leader in school search. our mission is to make researching and enrolling in schools easy, transparent, and free. with in-depth profiles on every school and college in america, 140 million reviews and ratings, and powerful search tools, we help millions of people find the right school for them. we also help thousands of schools recruit more best-fit students, by highlighting what makes them great and making it easier to visit and apply. niche is all about finding where you belong, and that mission inspires how we operate every day. we want niche to be a place where people truly enjoy working and can thrive professionally. about the role weʼre looking for a driven, resourceful, and experienced senior software engineer to join the data-driven content team, focused on enriching and scaling thesystems that power discovery and instill trust for our millions of users. collaborating closely with data engineering, product, and design, you will be taskedwith building services and user-facing features across our platform, with a strong focus on reliability, maintainability, scalability, testability, and userexperience. youʼll leverage your expertise spanning the entire stack, from database interactions to front-end libraries, contributing significantly to ourtechnical direction while mentoring other engineers. this is an ideal role for engineers who enjoy prototyping and experimenting to learn quickly. what you will do design, develop, and maintain robust and scalable full-stack applications and features acro...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
The master data analyst will be responsible for managing and continuously improving the global master data function , ensuring business continuity and enhancing analytics through clean and trustworthy data. this role involves custodianship of global master data including business partners, material master records, product hierarchies, boms, production versions, source lists, and purchasing info records in sap ecc/mdg. the analyst will lead data cleansing, transformation, and remediation efforts across multiple business processes (source to pay, order to cash, record to report, production planning). they will develop and maintain business rule books, audit compliance with governance standards, and utilize advanced analytics to drive business performance improvements. additionally, they will support automation initiatives and collaborate cross-functionally with procurement, it, and business stakeholders. this role requires a proactive individual capable of influencing and driving change, with a high attention to detail, a structured mindset, and a passion for data excellence. requirements bachelor’s degree in industrial engineering, computer science, mechanical engineering, business administration, supply chain management, or information systems . minimum of 3 years of experience with sap master data management and production planning. expertise in sap eim tools (mdg, netweaver mdm). proven experience in data visualization tools (power bi, tableau, sap bw). strong background in data quality management tools (information steward, informatica). advanced understand...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
We’re hiring! senior backend engineer – bogotá (hybrid) at traffic tech , we’re transforming global freight logistics with intelligent, scalable platforms that power the movement of goods worldwide. our bogotá tech hub partners closely with teams across north america, europe, and asia to advance our freight operating system . we’re looking for a senior backend engineer to design, implement, and maintain our core services and data pipelines . you will take ownership of high-performance, scalable back-end systems that support our freight management workflows. strong devops skills—such as building ci/cd pipelines, automating infrastructure, and implementing observability—are highly desirable to ensure smooth deployment and operation of your services. location : bogotá, colombia – hybrid language requirement : english (b2+) – mandatory what you bring 5+ years building backend systems in python (fastapi, django) with postgresql and kafka proven experience with event-driven architectures and data pipelines strong skills in async programming and data validation (pydantic) expertise in restful and grpc api design, authentication, and versioning english proficiency (b2+), spoken and written problem-solving mindset and ability to work autonomously in hybrid, multicultural teams nice to have ci/cd experience with github actions, argocd, or jenkins kubernetes (aks) and azure cloud knowledge familiarity with observability stacks and secops best practices certifications (ckad, azure devops, cloud security) background in logistics, transportation, or supply chain what you’ll do ba...
Wolf is seeking a detail-oriented, curious, and resourceful lead generation & data specialist to help us fuel growth by identifying and managing the right opportunities. in this role, you’ll combine research skills anddata management expertise to identify high-quality prospects, keep our crm in top shape, and provide the actionable intelligence our sales and marketing teams need to connect with the right people at the right time. you’ll be a critical player in expanding our reach and improving our targeting, working cross-functionally to ensure our lead pipeline is accurate, organized, and ready for high-impact campaigns. if you thrive on digging into data, spotting patterns, and delivering results that directly drive revenue, this is the role for you. about the role you'll play a key role driving outbound pipeline growth by generating and enriching lead data, and maintaining lead hygiene. partnering closely with sales and marketing, you’ll own building robust outreach-ready lists, maintain our crm (salesforce), and provide actionable intelligence to fuel targeted campaigns and outreach strategies. key responsibilities research & prospecting : identify target leads and contacts using web, database, and social research (e.g., linkedin sales navigator, apollo.io , zoominfo). data enrichment & maintenance : clean, verify, and enrich lead records—ensuring accuracy in titles, emails, company info, and contact data. database management : manage salesforce—ensure data is properly tagged, segmented, and up to date. lead qualification : score leads against defined icp criteria...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist - 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), ac...
Improvado is an ai-powered, unified platform designed for marketing teams in medium to large-scale enterprises and agencies, who are looking to automate complex marketing intelligence and reporting to make decisions with ease. improvado gathers, organizes, and untangles marketing data to deliver instant insights through bi and ai, helping to eliminate complexity, delivering laser-focused insights to optimize budgets, enhance campaign efficiency and marketing roi. as a rapidly scaling series a startup that raised $34 million in funding, we're proud to partner with globally recognized brands such as asus, docker, activision, h&r block, and many others. our diverse team of curious, open, and hard-working individuals is committed to cultivating a fast-paced, agile culture that values personal and professional growth. about the role we're looking for a hands-on ai principle engineer to help us build the future of ai at improvado. it’s a unique opportunity for someone excited to define the product vision based on real user needs and directly build the systems that power it. you’ll work closely with our ceo (who’s also our chief product officer with a strong technical background) to drive the direction of our ai features. from high-level strategy to low-level implementation, you’ll bridge product thinking and deep engineering. you'll also help guide a small, talented team of ai engineers — mentoring, setting direction, and writing production code alongside them. note: this is a high-ownership, high-impact role with a 6-day workweek. we’re building fast and need someone ready to mo...
We’re looking for a senior data engineer to design, build, and maintain the data foundation behind our next-generation ai agent platform. you’ll work closely with ai/ml teams to power training, inference, and continuous learning through highly scalab...
Who we are we are a fast-growing vertical saas company that leverages innovation and disruptive technologies to improve consumer experiences, outcomes, and predictability in elective medicine. our team thrives on challenges, embraces change, and is d...
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