Senior Clinical Data Manager - Flexible, Home-Based

Indero (formerly Innovaderm); Buenos Aires; Presencial; ARS 15.713.000 - 26.713.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible work schedule

Permanent full-time position

Ongoing learning and development

Descripción de la vacante

Indero (formerly Innovaderm) is seeking a Senior Clinical Data Manager to lead multiple clinical studies, ensuring data are collected, managed and reported clearly, accurately and securely. The role requires adherence to regulatory requirements, industry guidelines, and SOPs while aligning with sponsor timelines.

You will act as the data management liaison to project teams, sponsors and vendors, managing 3–4 concurrent studies with minimal supervision and developing eCRF specifications and study

Formación

• B.Sc. or related field required.
• M.Sc. or related field is an asset.
• 5–8 years of clinical data management experience in biotech/pharma/CRO.
• Understanding of drug development and GCP/ICH guidelines.
• Extensive experience with EDC systems and database structures.

Responsabilidades

• Serve as data management liaison to the project team, sponsor, and vendors.
• Manage 3–4 concurrent studies independently with minimal supervision.
• Develop eCRF specifications and the study-specific clinical database/EDC system.
• Program and maintain the clinical database; validate and test the database (UAT).
• Develop data management plans and training materials; train site users/monitors.

Conocimientos

Liaison & coordination

Attention to detail

Project management

Communication in English

French language (asset)

Educación

B.Sc. or related field

M.Sc. or related field (asset)

Herramientas

MS Excel

SAS (asset)

EDC systems

Descripción del empleo

Indero (formerly Innovaderm) is seeking a Senior Clinical Data Manager to lead multiple clinical studies, ensuring data are collected, managed and reported clearly, accurately and securely. The role requires adherence to regulatory requirements, industry guidelines, and SOPs while aligning with sponsor timelines.

You will act as the data management liaison to project teams, sponsors and vendors, managing 3–4 concurrent studies with minimal supervision and developing eCRF specifications and study