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ICON plc

Clinical Data Science Lead

ICON plc

. Develop and oversee the timeliness of clinical data science activities during the life cycle of studies as they relate to data review and data delivery milestones .

Posted 9/24/2026full-timeMexico City • MexicoSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in clinical data management, including proficiency in Clinical Data Management systems and a strong understanding of the data science lifecycle. Capable of leading projects, managing timelines, and ensuring data integrity while collaborating with cross-functional teams.

Highest-signal resume keywords
Clinical Data ManagementData Science LifecycleMedidata RaveData AnalyticTimeline Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Data ManagementData AnalyticData ValidationProject ManagementBudget ForecastingData ReviewClinical Risk ManagementAnalytic ReviewTimeline NegotiationCross-Functional Collaboration
Soft Skills
Excellent Communication Skills
Tools & Technologies
Medidata RaveInformOracle ClinicalVeeva
Industry Keywords
Clinical Research OrganizationPharmaceutical CompanySponsor AuditsThird-Party AuditsOperational Plans

Tech Stack

Tools & technologies
Oracle

About the role

Key responsibilities & impact
  • Develop and oversee the timeliness of clinical data science activities during the life cycle of studies as they relate to data review and data delivery milestones
  • Negotiate timelines and key deliverables with clients, external customers, vendors, and departments
  • Participate in sponsor and/or third-party audits
  • Forecast budget, hours, and resourcing for clinical data review activities
  • Perform analytic review focusing on errors that matter or meaningfully impact subject safety or final analysis interpretation
  • Work and collaborate with cross-functional and global groups
  • Provide input into clinical system development and clinical risk management activities
  • Develop planning documents related to data review, data analytics, and data deliverables
  • Establish approaches and lead resources to achieve operational and strategic plans
  • Track and communicate issues affecting project target dates, scope, or budget, escalating potential problems effectively and promptly
  • Apply existing procedures and analyze information and standard practices to make judgment calls
  • Travel approximately 15% domestically and/or internationally

Requirements

What you’ll need
  • 4+ years of clinical data management experience in a clinical research organization or pharmaceutical company
  • Experience leading multiple projects simultaneously
  • Experience with all steps within the data science lifecycle and most major data science study tasks
  • Proficiency in at least one Clinical Data Management system required, such as Medidata Rave, Inform, Oracle Clinical, or Veeva
  • Excellent communication skills
  • Timeline management experience
  • Data Analytic and Data Validation experience
  • Bachelor’s degree or local equivalent
  • Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above
  • Fluent English and host country language, including reading, writing, and speaking
  • Legal right to work in the country where the role is based

Benefits

Comp & perks
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways