Remote Clinical Data Coordinator – Drive Trial Quality

ICON Strategic Solutions; Ciudad de México; Presencial; MXN 420.000 - 660.000; Jornada completa

Descripción de la vacante

ICON plc in Mexico offers a remote opportunity for a CDC I to design and analyse clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments and therapies.

As part of the role you will take responsibility for clinical research deliverables, develop eCRF and data validation specifications, review data against edit specs, and issue clear queries to investigator sites, collaborating with data scientists and cross-functional teams to keep studies on

Formación

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

Responsabilidades

• Assist Data Management Study Lead in developing eCRF, Data Validation Specifications and Study Specific Procedures.
• Review data based on edit specifications and data review plans.
• Issue clear, accurate queries to investigational sites.
• Communicate effectively with peers, clinical data scientists and management.
• Support study timelines by performing related activities (documentation, query dispatch, etc.).

Conocimientos

Attention to detail

Communication skills

Collaboration

ICH-GCP knowledge

Educación

Bachelor's degree in Life Sciences or Healthcare

Herramientas

Medidata

Oracle RDC

Descripción del empleo

ICON plc in Mexico offers a remote opportunity for a CDC I to design and analyse clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments and therapies.

As part of the role you will take responsibility for clinical research deliverables, develop eCRF and data validation specifications, review data against edit specs, and issue clear queries to investigator sites, collaborating with data scientists and cross-functional teams to keep studies on