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Job summary
Google Cloud is seeking a Data Customer Solutions Engineer to design, deploy, and manage scalable databases across Google Cloud Platform. You will lead data migrations, implement governance, and collaborate with product teams to improve database solutions for customers globally.
The role requires strong programming skills (Python, Java), SQL/NoSQL experience, and the ability to communicate in English and Spanish/Portuguese for LATAM stakeholders. Travel to customer sites is expected.
Qualifications
- Bachelor's degree in Engineering, Computer Science, a related field, or equivalent practical experience.
- Experience coding with one or more programming languages (e.g., Java, C/C++, Python).
- Experience in developing and troubleshooting applications with databases such as MySQL, PostgreSQL, Oracle, and NoSQL databases like MongoDB.
- Experience with Structured Query Language (SQL).
- Bachelor's degree with 5 years of technical troubleshooting (preferred).
- Proficiency in data modeling, distributed systems, and SQL/NoSQL and Google Cloud databases (Spanner, BigTable, AlloyDB).
- Expertise in large-scale data migrations from on-premise to cloud.
- Strong programming skills (Python, Java), CI/CD and IaC tooling.
- Knowledge of data protection, encryption (KMS, HSMs), and regulatory compliance (GDPR, CCPA, HIPAA).
- Ability to communicate in English and Portuguese/Spanish for LATAM stakeholders.
Responsibilities
- Translate complex business and technical requirements into scalable database solutions and advisory services.
- Lead high-velocity data migration and modernization to Google Cloud Platform.
- Develop data quality and governance procedures ensuring data accuracy.
- Troubleshoot storage systems with customers or partners for performance issues.
- Organize requirements into clear goals and a work breakdown structure.
Skills
Education
Tools
Job description
Data Customer Solutions Engineer, Google Cloud
Share Data Customer Solutions Engineer, Google Cloud
_corporate_fare_ Google _place_ Buenos Aires, Argentina; Mexico City, CDMX, Mexico
Early
Experience completing work as directed, and collaborating with teammates; developing knowledge of relevant concepts and processes.
XIn most instances, this position requires in-person interviews as part of the hiring process.
Only applications of candidates with Mexican citizenship will be evaluated for this role in compliance with the provisions of Article 7 of the Federal Labor Law.
Note: By applying to this position you will have an opportunity to share your preferred working location from the following: Buenos Aires, Argentina; Mexico City, CDMX, Mexico.
- Bachelor's degree in Engineering, Computer Science, a related field, or equivalent practical experience.
- Experience coding with one or more programming languages (e.g., Java, C/C++, Python).
- Experience in developing and troubleshooting applications with popular database management systems such as MySQL, PostgreSQL, Oracle, and NoSQL databases like MongoDB.
- Experience with Structured Query Language (SQL).
- Bachelor's degree with 5 years of technical troubleshooting.
- Proficiency in data modeling, distributed systems, and SQL, NoSQL, and Google Cloud databases (Spanner, BigTable, AlloyDB).
- Expertise in designing and executing large-scale data migrations from on-premise systems to the cloud.
- Strong programming skills (Python, Java), script automation, and DevOps implementation using CI/CD and IaC tools.
- Deep understanding of data protection, encryption techniques (KMS, HSMs), and regulatory compliance (GDPR, CCPA, HIPAA).
- Ability to communicate in English and Portuguese/Spanish fluently for LATAM stakeholders.
As a Strategic Cloud Data Engineer, you will work with customers and partner teams to design, develop, deploy and manage highly scalable and reliable databases on the Google Cloud Platform meeting the Organization's storage demands. You will work on data migrations and modernization projects incorporating best practices of data governance and security controls. You will travel to customer sites to deploy solutions and deliver workshops to educate and empower customer teams to adhere to best practices in Database design and operations. Additionally, you will work closely with Product Management and Product Engineering teams to build and constantly drive excellence in our products that solve the biggest customer challenges.
Google Cloud accelerates every organization's ability to digitally transform its business and industry. We deliver enterprise-grade solutions that leverage Google's cutting-edge technology, and tools that help developers build more sustainably. Customers in more than 200 countries and territories turn to Google Cloud as their trusted partner to enable growth and solve their most critical business problems.
- Interact with stakeholders to translate complex business and technical requirements into recommendations for scalable and cost-effective database solutions and advisory services.
- Engage with technical leads and partners to lead high velocity data migration and modernisation to Google Cloud Platform (GCP) using Google or third-party tools and services.
- Develop and implement data quality and governance procedures to ensure the accuracy and reliability of data.
- Work with customer or partner teams to troubleshoot their complex storage systems for potential performance challenges.
- Take various project requirements and organize them into clear goals and objectives, and create a work breakdown structure to manage internal and external stakeholders.
Information collected and processed as part of your Google Careers profile, and any job applications you choose to submit is subject to Google's Applicant and Candidate Privacy Policy (./privacy-policy).
Google is proud to be an equal opportunity and affirmative action employer. We are committed to building a workforce that is representative of the users we serve, creating a culture of belonging, and providing an equal employment opportunity regardless of race, creed, color, religion, gender, sexual orientation, gender identity/expression, national origin, disability, age, genetic information, veteran status, marital status, pregnancy or related condition (including breastfeeding), expecting or parents-to-be, criminal histories consistent with legal requirements, or any other basis protected by law. See also Google EEOPolicy, Know your rights: workplace discrimination is illegal, Belonging at Google, andHow we hire.
If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form.
Google is a global company and, in order to facilitate efficient collaboration and communication globally, English proficiency is a requirement for all roles unless stated otherwise in the job posting.
To all recruitment agencies: Google does not accept agency resumes. Please do not forward resumes to our jobs alias, Google employees, or any other organization location. Google is not responsible for any fees related to unsolicited resumes.
Equity is granted exclusively and discretionarily by Alphabet Inc. on the basis of an agreement concluded between you and Alphabet Inc. Alphabet Inc. is your sole contractual partner with respect to equity grants. GSU grants are not guaranteed, are discretionary, are subject to approval by the Alphabet Inc. board of directors or its delegate, the terms of the relevant Alphabet Inc. stock plan, and your grant agreement. They have no impact on statutory payments. Current or past grants do not confer an acquired right.
Google is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. See also and If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form:
Buenos Aires, Buenos Aires, Argentina
Full time
GBS Chevron Global Business Services (GBS), located in Buenos Aires (Puerto Madero), Argentina, is accepting applications for the position of Data Engineer. Successful candidates will join the IT Organization, which is part of a multifunction service and technical center with a workforce of more than 1800 employees that deliver business services and solutions to the corporation across the globe.
Utilizes software engineering principles to deploy and maintain fully automated data transformation pipelines that combine a large variety of storage and computation technologies to handle a distribution of data types and volumes in support of data architecture design.
- Understand business use of data and stakeholder requirements to support work processes and strategic business objectives.
- Leverage data, software engineering, and data science techniques to create business value through data accessibility. Includes data ingestion, data preparation and analytics processing.
- Identify, acquire, cleanse & prepare, store data and develop data products aligned with defined architecture patterns.
- Responsible for normalizing and ingesting data from multiple sources.
- Enable data scientists, making data available for advanced analytics models, and contributing to models.
- Work with ML Engineer to scale and deploy solution including model, documentation, training, integration.
- Contributing to the inner source development of foundational tools, and/or the deployment of technical services.
- BS in Computer Science, Management Information Systems, Computer Engineer or related fields or equivalent experience.
- +5 years in Data Engineer Role.
- Knowledge and/or experience with: data acquisition, preparation and validation; data movement and transformation; analytics solution architecture; big data computing; cloud computing, core data architecture; information security technologies and software engineering using technologies such as: Azure Data Factory (ETL), Databricks, DevOps, CI/CD Pipeline Deployment, Python, Java, Ansible, Azure SQL, Azure Synapse, GIT, ADO, Azure Data Lake, Azure Analysis Services, Logic Apps, Microsoft Data Flows, Kimball Data Warehousing Methodology.
- Analytical thinking, Consulting, Critical Thinking.
Relocation may be considered.
Expatriate assignments will not be considered.
Chevron regrets that it is unable to sponsor employment Visas or consider individuals on time-limited Visa status for this position. Chevron participates in E-Verify in certain locations as required by law. Chevron is an Equal Opportunity / Affidavit Action employer.
Chevron Corporation is a leading integrated energy company with activities spanning crude oil production, gas, refining, marketing and distribution, petrochemicals, power generation, and technology development.
Buenos Aires, Argentina
São Paulo, Brazil
Full time
We are looking for a Medical Data Review Manager to join our team! Home based - global scope position. Specialization in Rehumatology (certified - mandatory). Review structured clinical patient data output without direct access to medical charts to ensure medical plausibility and determine adherence to protocol and overall completeness and readiness for next level of review.
- Identify any anomalies in patient reported data that require further investigation with the clinical site to determine overall accuracy.
- Review all inclusion and exclusion criteria to ensure each patient meets minimum level of acceptance into the clinical trial.
- Review investigation product dosing records to determine adherence to protocol and identify possible inaccurate / missed dosages.
- Review all reported Adverse Events (AEs), Concomitant Medication and medical history information to ensure all supporting information is expected and/or implausible data is verified and adherence to protocol expectations and its impact on other patient reported/observed information (e.g., laboratory results, AEs, etc.).
- Ensure end-of-treatment (EOT) and end-of-study (EOS) information is correctly documented to determine primary reason for the patient ending treatment or ending participation in the clinical trial.
- Review all laboratory results to ensure completeness of information and adherence to protocol schedule of events and determine if reported laboratory values represent a potential safety condition not reported in the AE information for the patient.
- Review any other information as necessary to determine overall readiness of the patient information for next level review.
- Interaction with other Medical review staff to verify information and/or triage new data issues or prior identified action items.
- Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
- Bachelor's Degree in Medicine, graduated and specialized in Rehumatology (mandatory - we can only consider physicians for this role).
- 5 years of related experience in clinical research - research site level or CRO/Pharmaceutical companies. Experience as Sub-Investigator or Principal Investigator are relevant.
- Advanced English level - great communication skills in the language. The role has a global scope.
- Understanding of clinical/medical data related to clinical trials.
- Background in Medical Terminology, Pharmacology, Anatomy, and Physiology.
- Excellent motivational, influencing and coaching skills.
- Ability to work on multiple projects and manage competing priorities.
- Strong customer focus skills.
- Ability to establish and maintain effective working relationships with coworkers, managers and clients.
IQVIA is a global provider of clinical research services and healthcare data intelligence. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes worldwide.
EEO Minorities/Females/Protected Veterans/Disabled
Mexico City, Mexico
Buenos Aires, Argentina
São Paulo, Brazil
Bogota, Colombia
Full time
Independently manage end-to-end delivery of data management services for single/multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet customer needs. Provide leadership and vision to the team in the areas of project planning, execution, and close-out; financial management; communications; and milestone deliverables. May perform role of Data Team Lead (DTL), Program Lead, Customer Site Manager, and/or a leadership role in a specific CDM task (e.g., Subject Matter Expert (SME)). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents.
- Client Management: Serve as primary point of contact for customer on data management deliverables.
- Manage multiple large studies or program of studies (possibly global) Provide leadership and senior support to DTLs on multiple large global studies/programs of global studies Provide leadership and senior support to DTLs on multiple large global studies/programs of global studies.
- Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise.
- Lead direct negotiations with customer, e.g., timelines, financial, process, resources.
- Maintain strong customer relationships.
- Ensure open communications with customer and IQVIA management to independently manage and meet contractual obligations.
- Service Management: Meet with Data Operations Coordinator (DOC) and/or Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables.
- Provide training and development on data management expertise to junior team members.
- Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders.
- Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projects.
- Serve as the escalation point for unresolved data issues.
- Independently work with client data managers, vendors, internal team members for resolution.
- Ensure appropriate resources are assigned to meet project deliverables.
- Create and/or review and sign-off on all data management plan (DMP) documents.
- Ensure service and quality meet agreed upon specifications per the DMP and contract/SOW.
- Implement proactive quality management plans across multiple projects/programs/customer account. Manage service performance and provide leadership to identify root causes of issues and implement remedial actions.
- Continuously look for opportunities to improve service.
- Develop and work with team to implement plan to re‑organize and drive change (possibly across a customer account).
- Ensure timely follow-up and resolution of compliance issues.
- Serve as Subject Matter Expert (SME).
- Provide leadership and expertise in a specific CDM task or technology.
- Serve as customer site lead for one or more customers.
- Train and mentor junior DTL staff in DM expertise.
- May coordinate the work of more junior DTL staff.
- Independently maintain internal tracking databases and systems.
- Independently manage SOW/budget.
- Review financial reports monthly and participate in project reviews as requested.
- Identify out of scope tasks and track change orders to completion.
- Participate in pricing discussions across customer account.
- Serve as Project Manager for single service DM projects, including financial tracking, revenue recognition, and invoicing.
- Independently support RFP process (review RFP documents, pricing, attend bid defense).
- Independently bring process improvements and solutions to the CDM team/CDM department.
- Lead a focus team or global or local best practice team.
- Communicate lessons learned and/or present in CDM workshop(s).
- Manage the development and implementation of new technology or tool.
- Present at professional conferences and/or publish articles in professional journals.
- Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions.
- Perform other duties as directed by the functional manager.
Please note that requirements for this position do not align with an Analyst, Architect Data Entry, Design, Engineering, IT, or Research role. Applicants that do not meet the requirements for the position will not be considered.
- Bachelor's Degree Health, clinical, biological, or mathematical sciences, or related field Req.
- 7 years direct Data Management experience, including 5 or more years as a CDM project lead. Equivalent combination of education, training, and experience.
- Previous experience and proven competence in managing delivery of multiple global trials through full DM life cycle (i.e., large trials of at least 1000 patients).
- Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation, management of local laboratory data, and/or new technology).
- Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently. Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology.
- Knowledge of operating procedures and work instructions and the ability to apply them in practice.
- Knowledge of Good Clinical Practices and relevant regulatory guidelines.
- Comprehensive understanding of clinical drug development process.
- Ability to establish and maintain effective working relationships with coworkers, managers and customers.
- Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology.
EEO Minorities/Females/Protected Veterans/Disabled
Standard (Mon-Fri)
Office
Join Us as a Senior Clinical Data Associate - Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our expert team, you'll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Senior Clinical Data Associate, you will perform all aspects of the data cleaning process, with minimal supervision, in accordance with Good Clinical Practices (GCP) and Standard Operating Procedures/Work Process Documents (SOPs/WPDs), to assess the safety and efficacy of investigational products and/or medical devices.
- Supports the setup of study activities such as database design, testing of data entry screens, and Data Validation Manual (DVM) creation, as required.
- Reviews data listings for accuracy and consistency of data.
- Acts as point person and subject matter expert for specialized study-specific processes.
- Generates, tracks and resolves data clarifications and queries and makes changes to the clinical database as required.
- Contributes to the improvement of data management processes on a global level.
- Produces project-specific status reports for management and/or clients on a regular basis.
- Provides training and work direction to junior staff as required.
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification.
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
- In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
- Applies knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations.
- Strong attention to detail and skill with numbers.
- Good written and verbal communication skills.
- Good analytical/problem-solving skills.
- Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data.
- Strong customer focus and excellent interpersonal skills.
- Proven flexibility and adaptability.
- Must be able to set and meet timelines or be able to negotiate schedule changes in response to project demands.
- Knowledge of medical/clinical terminology.
- Understands project protocol and DVM.
- Proven ability in achieving applicable technical competencies per the DM competency grid.
- Work is performed in an office environment with exposure to electrical office equipment.
- Occasional drives to site locations.
- Occasional travel both domestic and international.
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
Office
Join Us as a Senior Clinical Data Team Lead - Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our expert team, you'll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Senior Clinical Data Team Lead, you will act as a lead data manager for one or more projects and serve as a liaison to the Project Lead and/or client as required.
- Applies relevant components of the project protocol to daily tasks and directs others on how to apply to their daily tasks.
- Acts as an interdepartmental and client liaison for all DM study activities.
- Produces project-specific status reports for management, Project Lead and/or clients on a regular basis.
- Monitors and analyzes study metrics and escalates per the organization's risk management processes.
- May participate in business development activities by assisting with bid preparation and representing data management at bid defense meetings, where required.
- Assists with project forecasting of hours and identification of resource requirements.
- Assists with the oversight of project budgets including identification of potential out of scope work and participation in the Contract Modification process.
- Leads, high volume/highly complex studies.
- Independently leads and delegates tasks to ensure timely completion of project activities to project timelines, quality and budget.
- Mentors junior level staff on all associated tasks within a study.
- Assists with the administration and financial oversight for allocated projects.
- Communicates with management regarding all data management activities within their studies.
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification.
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
- In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
- Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, SOPs and client expectations.
- Ability to use interactive computer programs.
- Good written/ verbal communication skills with a strong command of English language and grammar; good organizational, analytical/problem solving skills and attention to detail.
- Ability to work productively in both a team environment and independently as needed.
- Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data.
- Strong customer focus and excellent interpersonal skills.
- Ability to direct and train study team.
- Ability to act as a study or department expert for DM processes.
- Ability to support project resourcing and project timeline planning and adherence to timelines.
- Work is performed in an office environment with exposure to electrical office equipment.
- Occasional drives to site locations with occasional travel both domestic and international.
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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