Remote Clinical Data Coordinator - Trials & QC

ICON Clinical Research; México; A distancia; MXN 420.000 - 660.000; Jornada completa

Descripción de la vacante

ICON plc, a world-leading healthcare intelligence and clinical research organization, seeks a CDC I to design and analyse clinical trials, interpreting complex medical data and contributing to innovative treatments.

You will take responsibility for clinical research deliverables, review data, generate queries, and support study timelines in a fast-paced, collaborative environment while ensuring adherence to ICH-GCP and regulatory guidelines.

Formación

• Bachelor's degree or equivalent in Life Sciences or Healthcare.
• Basic knowledge of clinical data management within pharma/biotech.
• Familiarity with data management software and systems (Medidata, Oracle RDC).
• Strong attention to detail and ability to work in a fast-paced environment.
• Excellent communication and collaboration across cross-functional teams.
• Knowledge of regulatory guidelines (ICH-GCP) is a plus.

Responsabilidades

• Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures.
• Review clinical and third-party data based on edit specs and data review plans.
• Issue clear, concise queries to investigational sites.
• Communicate effectively with peers, clinical data scientist and management.
• Perform other project activities to ensure study timelines are met.

Conocimientos

Data management knowledge

Medidata/Oracle RDC familiarity

Attention to detail

Strong communication skills

ICH-GCP knowledge

Educación

Bachelor's degree in Life Sciences or Healthcare

Herramientas

Medidata

Oracle RDC

Descripción del empleo

ICON plc, a world-leading healthcare intelligence and clinical research organization, seeks a CDC I to design and analyse clinical trials, interpreting complex medical data and contributing to innovative treatments.

You will take responsibility for clinical research deliverables, review data, generate queries, and support study timelines in a fast-paced, collaborative environment while ensuring adherence to ICH-GCP and regulatory guidelines.