Remote Principal Clinical Data Scientist, CSAI Analytics

Precision for Medicine

México

Híbrido

MXN 1.200.000 - 2.000.000

Jornada completa

14 días+
Generador de candidaturas

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Descripción de la vacante

Precision Medicine Group seeks a Principal Clinical Scientist in CSAI to manage operational clinical science across studies, focusing on data capture, cleaning, and visualization. You will serve as the scientific subject matter expert applying clinical knowledge and standards to trial data.

You will lead CSAI service delivery, collaborate with data management, medical, safety, and vendors, and help develop study documentation and eCRF specifications.

Formación

  • Bachelor’s degree or equivalent combination of education/experience in science or health-related discipline with proficiency in medical terminology.
  • Minimum of 8 years of clinical research experience or proven competencies for this position.
  • Minimum of 1 year of leadership experience.

Responsabilidades

  • Serve as the functional lead implementing CSAI services per study scope of work (SOW) on assigned project team(s).
  • Serve as a resource for project teams regarding scientific related data capture, review & cleaning.
  • Support and participate in the development and implementation of process flow for integrated data cleaning across departments.
  • May manage cross-functional data cleaning to support interim/final data deliverables.

Conocimientos

Leadership experience
Strong communication
English proficiency
Cross-functional collaboration
Regulatory knowledge

Educación

Bachelor’s degree or equivalent in science/health discipline

Herramientas

JReview
EDC systems
Microsoft Office

Descripción del empleo

Precision Medicine Group seeks a Principal Clinical Scientist in CSAI to manage operational clinical science across studies, focusing on data capture, cleaning, and visualization. You will serve as the scientific subject matter expert applying clinical knowledge and standards to trial data.

You will lead CSAI service delivery, collaborate with data management, medical, safety, and vendors, and help develop study documentation and eCRF specifications.

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