Remote Global Data Migration Lead For Erp (S/4Hana)

Randstad Argentina; Buenos Aires; Remoto; ARS 139.086.000 - 185.448.000; Tempo pieno

Vantaggi offerti da questo lavoro

Connectivity allowance

Gym reimbursement

PedidosYa credit

Statutory vacation

Health insurance: Swiss Medical or OS

Descrizione del lavoro

Randstad Argentina is looking for a Senior Data Migration Lead to drive end-to-end planning and execution of a data migration program for a global automotive manufacturer. You will coordinate cross-functional teams, define migration approach and controls, and manage risks to ensure a smooth transition to the target system.

The role requires proven data migration leadership in large enterprise programs, strong methodology knowledge, and experience with ERP migrations (S/4HANA preferred).

Competenze

• Proven experience as a Data Migration Lead or Team Lead in large-scale enterprise programs.
• Strong knowledge of data migration methodology: extraction, transformation, cleansing, validation and loading.
• Experience coordinating cross-functional teams across multiple workstreams.
• Ability to define migration controls and risk management strategies.
• Experience working in S/4HANA or similar ERP migration programs (preferred).
• Intermediate to advanced English — interviews and daily work conducted in English.
• Availability to work in UTC timezone (9:00 AM – 5:00 PM).

Mansioni

• Lead the end-to-end planning and execution of data migration activities.
• Ensure data is accurate, complete, and ready for use in the target system.
• Coordinate cross-functional migration teams across workstreams.
• Define the data migration approach, methodology and quality controls.
• Identify, assess and manage migration risks and issues.
• Ensure a smooth and reliable transition with minimal disruption.
• Report migration status and progress to senior stakeholders.

Conoscenze

Data migration leadership

Data migration methodology

Cross-functional coordination

Migration controls & risk mgmt

ERP migration (S/4HANA)

English proficiency

UTC timezone availability

Descrizione del lavoro

100% Remote Full-time

️ English: Intermediate/Advanced (required — interviews conducted in English) | 9:00 AM – 5:00 PM UTC

️ CVs must be submitted in English

About the Role

Join the team supporting one of the world's largest automotive manufacturers, working within a global consulting firm to lead the planning and execution of a critical data migration program. You will coordinate cross‑functional teams, define the migration approach and controls, and manage risks to ensure a smooth and reliable transition to the target system.

Responsibilities

• Lead the end‑to‑end planning and execution of data migration activities
• Ensure data is accurate, complete, and ready for use in the target system
• Coordinate cross‑functional migration teams across workstreams
• Define the data migration approach, methodology and quality controls
• Identify, assess and manage migration risks and issues
• Ensure a smooth and reliable transition with minimal disruption
• Report migration status and progress to senior stakeholders

Required Skills

• Proven experience as a Data Migration Lead or Team Lead in large‑scale enterprise programs
• Strong knowledge of data migration methodology: extraction, transformation, cleansing, validation and loading
• Experience coordinating cross‑functional teams across multiple workstreams
• Ability to define migration controls and risk management strategies
• Experience working in S/4HANA or similar ERP migration programs (preferred)
• Intermediate to advanced English — interviews and daily work conducted in English
• Availability to work in UTC timezone (9:00 AM – 5:00 PM)

Hiring Process

• Collaborative environment with high‑impact projects across leading industries
• Connectivity allowance
• Gym reimbursement
• PedidosYa credit
• Statutory vacation
• Health insurance: Swiss Medical or OSDE

Mexico City, Mexico
Buenos Aires, Argentina
São Paulo, Brazil
Bogota, Colombia
Full time
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Job Overview

+ 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.

Essential Functions

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
Financial Management/Business Development Support:
+ 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)
Other:
+ 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.
**Qualifications**
+ 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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Qualifications

+ Bachelor’s degree in Life Sciences, Healthcare, or a related scientific discipline
+ 5+ years of clinical research, monitoring, or clinical operations experience within a CRO, pharmaceutical, or biotechnology environment
+ Strong understanding of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements
+ Experience leading clinical study delivery activities, including patient recruitment, site management and clinical quality oversight
+ Proven ability to collaborate across cross‑functional teams and manage internal and external stakeholders in a global environment
+ Strong communication, problem‑solving, organizational and decision‑making skills
+ Experience supporting project financial management and operational planning is desirable
+ Passion for advancing clinical research and improving outcomes for patients worldwide

EEO Minorities/Females/Protected Veterans/Disabled

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

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.
**What You'll Do:**
• 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 administrative and financial oversight for allocated projects.
• Communicates with management regarding all data management activities within their studies.
**Education and Experience Requirements:**
• 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.
**Knowledge, Skills and Abilities:**
• 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 an 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
• Working Conditions and Environment:
• 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.
Why Join Us?
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.
Apply today to help us deliver tomorrow's breakthroughs.
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.

Benefits

We take care of you, so you can take care of business. We care about our people. That's why we provide everything you-and your career-need to thrive at S&P Global.
Our benefits include:

• Health & Wellness: Health care coverage designed for the mind and body.
• Flexible Downtime: Generous time off helps keep you energized for your time on.
• Continuous Learning: Access a wealth of resources to grow your career and learn valuable new skills.
• Invest in Your Future: Secure your financial future through competitive pay, retirement planning, a continuing education program with a company-matched student loan contribution, and financial wellness programs.
• Family Friendly Perks: It's not just about you. S&P Global has perks for your partners and little ones, too, with some best-in-class benefits for families.
• Beyond the Basics: From retail discounts to referral incentive awards-small perks can make a big difference.