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Technical Data Analyst

ICON Plc

México

A distancia

USD 25,000 - 35,000

Jornada completa

Ayer
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Descripción de la vacante

A leading healthcare intelligence organization is seeking a Technical Data Analyst in Mexico City. This remote role involves supporting imaging science and project management, ensuring data quality, and collaborating with clients. The ideal candidate will have experience in data coordination within the pharmaceutical industry, strong communication skills, and a relevant degree. Join ICON to help shape the future of clinical development while enjoying a diverse culture and competitive benefits.

Servicios

Annual leave entitlements
Health insurance options
Retirement planning
Global Employee Assistance Programme
Life assurance
Flexible benefits like childcare vouchers
Gym memberships

Formación

  • At least 1 year of experience in data coordination or analysis.
  • Current radiologic technologist certification required.

Responsabilidades

  • Assist in identifying data entry errors through reconciliation.
  • Perform quality control on source documents.
  • Lead Data Coordinator responsibilities for assigned protocols.

Conocimientos

Data coordination
Data analysis
Statistics
Biostatistics
Communication
Organization
Prioritization
Fluent in English

Educación

Bachelor's degree in health sciences

Descripción del empleo

Technical Data Analyst - Mexico City - Remote (Homeworker)

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

The Role:

The Technical Data Analyst supports Imaging Science, Project Management, and Radiology in the review and approval of image analysis for data delivery.

  • Assist in identifying data entry errors through reconciliation.
  • Perform quality control on source documents.
  • Review data file structure requirements with GDS Management and contact clients for clarification if needed.
  • Document all QC activities thoroughly.
  • Review image analysis accuracy performed by the medical team.
  • Resolve identified errors promptly.
  • Identify trends in documentation errors.
  • Assist in developing new methods for data entry and QC.
  • Review and QC source documents with eCRF or draft database.
  • Create data batches, perform QC checks, and transmit data files.
  • Lead Data Coordinator responsibilities for assigned Protocols, utilizing strong communication, organization, and prioritization skills.
  • Plan, develop, test, and document custom data file formats per client needs.
Qualifications:
  • At least 1 year of experience in Data coordination, analysis, statistics, or biostatistics within the pharmaceutical industry.
  • Knowledge of study designs and data analysis conventions.
  • Fluent in English (verbal and written).
  • Understanding of clinical trials methodology and regulatory requirements.
  • Preferred: Experience with clinical trials and regulated environments.
  • Experience in Imaging is a plus.
  • Bachelor's degree in health sciences or related field.
  • Current radiologic technologist certification and background in anatomy are required.

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What ICON can offer you:

We prioritize building a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, ICON offers various benefits focused on well-being and work-life balance, including:

  • Annual leave entitlements
  • Health insurance options
  • Retirement planning
  • Global Employee Assistance Programme, LifeWorks
  • Life assurance
  • Flexible benefits like childcare vouchers, gym memberships, and more

Visit our careers site for more information. ICON is committed to an inclusive, accessible environment and equal opportunity employment. If you need accommodations during the application process, please contact us.

We encourage all qualified candidates to apply, even if you don't meet every requirement. Current ICON employees can apply here.

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