Senior Principal Technical Data Specialist (LATAM)

Precision For Medicine; Colombia; Sur place; COP 220 000 000 - 380 000 000; Plein temps

Résumé du poste

Precision Medicine Group in Colombia and across the region is expanding its data management capabilities and seeks a Senior Principal Technical Data Specialist to lead enterprise data governance, strategy, and technical oversight.

You will define requirements, governance, architecture, testing standards, and oversee migrations, data integration, and archival across clinical data platforms, steering complex programs toward compliant, production-ready outputs.

Qualifications

• Bachelor’s degree with 12+ years in technical leadership for data management.
• Advanced degree or recognized leadership credentials preferred.
• Experience in enterprise strategy, governance, architecture, and compliance.

Responsabilités

• Define enterprise requirements quality and traceability.
• Govern CRF templates, design principles, and data transfer agreements.
• Establish architecture governance for database delivery and interoperability.
• Lead testing standards, validation, and archival practices.

Connaissances

Data governance

Technical strategy

Stakeholder influence

Leadership

Compliance

Formation

Bachelor’s degree

Advanced degree

Outils

EDC systems

Data integration platforms

Data governance tools

Description du poste

We’re expanding our data management capabilities across Mexico, Brazil, Argentina, Colombia, Chile, and Peru, and we’re hiring a Senior Principal Technical Data Specialist to help build the foundation of this new regional technical data management organization!

The Senior Principal Technical Data Specialist is the senior individual-contributor authority for Technical Data Management. The role shapes functional strategy and technical governance across strategic programs; defines enterprise expectations for requirements, specifications, architecture, testing, integration, migration, archival, and quality; and ensures programmed outputs align with approved requirements before production use.

The role directs resolution of the most complex or high-risk challenges, influences sponsor and internal technology decisions, develops technical capability across the function, and sponsors innovation and process transformation.

Main Duties & Responsibilities

• Protocol & Requirements Translation: Define enterprise expectations for requirements quality and traceability, advise on novel study designs, and resolve critical requirements issues across strategic programs.
• CRF, Edit Check & Technical Specifications: Provide governance for the full suite of technical specifications, shape and harmonize CRF-aligned templates and design principles across platforms, portfolios, and therapeutic areas, create data transfer agreements, and arbitrate high-impact technical design decisions.
• Database Design & Build Oversight: Establish technical architecture and governance expectations for database delivery, advising leadership on strategic design trade-offs, platform capabilities, interoperability, AI enablement, and systemic technical risk.
• Testing, Defect Management & Validation: Define technical testing standards and quality thresholds, provide assurance for critical validation issues, sponsor advanced automation, and establish expectations for technical execution and evidence while supporting overall coordination by the Lead Data Manager.
• Production Readiness, Migration, Change Control & Archival: Provide governance for major migrations, platform transitions, post-production change, and technical database archival within selected EDC systems; direct response to critical deployment or archival risk and define sustainable practices.
• Data Integration & Workbench Enablement: Shape integration and data-cleaning workbench strategy, long-term technical architecture, operating models, data lineage, control points, and interoperability across clinical data platforms.
• Quality, Compliance & Documentation / Cross-Functional & Sponsor Collaboration / Program Complexity, Planning & Risk Management / Mentoring, Standards & Continuous Improvement: Represent Technical Data Management in strategic governance and sponsor forums; define technical quality and inspection-readiness expectations; lead strategy for business-critical programs; build organizational capability; sponsor innovation and transformation; and ensure sustainable value.

Education And Experience

Minimum Education & Experience:

• Bachelor’s degree in a relevant discipline or equivalent training and experience; and typically 12+ years of relevant experience, including enterprise- or portfolio-level technical leadership and delivery of major improvements or transformations.

Preferred Education & Experience (optional)

• Advanced degree or recognized technical leadership credentials, together with demonstrated competencies in enterprise strategy, governance, architecture, compliance, and transformation.
• Or equivalent combination of education, professional training and experience that provides the individual with the required knowledge, skills, and abilities to perform the job.

Knowledge, Skills, And Competencies

• Recognized expert knowledge of technical clinical data strategy, governance, compliance, inspection readiness, and evolving industry practices.
• Broad and deep expertise across clinical data platforms, architecture, EDC, integrations, workbenches, data flows, standards, testing, migration, and archival.
• Ability to define enterprise requirements, specification, testing, quality, traceability, and technical governance expectations.
• Ability to shape technology strategy, technical architecture, library development, interoperability, AI enablement, and evaluation of emerging capabilities.
• Exceptional judgment and enterprise thinking when directing resolution of unprecedented or business-critical technical challenges.
• Ability to lead technical strategy for the most complex programs and inform capacity, capability, resourcing, and investment planning.
• Trusted strategic communication and the ability to influence senior stakeholders, sponsors, vendors, and major internal and external governance forums.
• Ability to define sustainable change-control, migration, platform-transition, archival, preventive-control, and inspection-readiness practices.
• Ability to build organizational technical capability, develop successors and technical leaders, sponsor innovation, and establish adoption measures.
• Exemplary technical leadership, ethical judgment, client focus, accountability, inclusive collaboration, professionalism, and sustained organizational impact.

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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [e-mail].

Candidates must be legally authorized to work in the country of employment without employer sponsorship.