Senior Clinical Data Manager - LATAM | Remote

Precision Medicine Group

México

A distancia

MXN 900.000 - 1.500.000

Jornada completa

hace 34 horas
Sé de los primeros/as/es en solicitar esta vacante
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Ventajas ofrecidas por este puesto de trabajo

Remote work

Descripción de la vacante

Precision Medicine Group is seeking an experienced Senior/Principal Clinical Data Manager to lead the data management lifecycle for LATAM trials, from start-up to database lock, ensuring high-quality data for successful trials and faster therapies.

You will oversee CRF specs, database builds, edit checks, data entry guidelines, and QA, while collaborating with sponsors, vendors, and cross-functional teams. 8+ years' experience and CDISC/MedDRA knowledge preferred.

Formación

  • Bachelor's degree or equivalent in a related field.
  • 8+ years of experience for Sr. Clinical Data Manager and 10+ years for Principal.
  • Proficiency with Microsoft Office: Word, Excel, PowerPoint, Outlook.
  • Experience with clinical database management systems and data standards (CDISC).

Responsabilidades

  • Lead data management contact for assigned projects, ensuring back-up and timely task execution.
  • Oversee data entry process, guidelines, training, and data quality.
  • Develop CRF specifications and coordinate stakeholder feedback.
  • Perform & oversee data quality checks, edit check specs, and QA of databases.
  • Train staff on CRF/EDC and project items; ensure TMF completeness.

Conocimientos

Lead DM
Data management
Project coordination
English proficiency
Communication
Travel readiness

Educación

Bachelor's degree

Herramientas

SAS
Microsoft Office

Descripción del empleo

Precision Medicine Group is seeking an experienced Senior/Principal Clinical Data Manager to lead the data management lifecycle for LATAM trials, from start-up to database lock, ensuring high-quality data for successful trials and faster therapies.

You will oversee CRF specs, database builds, edit checks, data entry guidelines, and QA, while collaborating with sponsors, vendors, and cross-functional teams. 8+ years' experience and CDISC/MedDRA knowledge preferred.

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