Remote Central Review Coordinator

Blacksmith Agency Llc; South Africa; A distancia; ZAR 350.000 - 700.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive salary

Annual leave entitlements

Health insurance options

Retirement planning offerings

Life assurance

Global Employee Assistance Programme

Descripción de la vacante

ICON Strategic Solutions is seeking a Central Review Coordinator to join the Central Review Services team. The role supports centralized endpoint data evaluation and data management for a major sponsor in a CRO setting.

The successful candidate will manage trackers, monitor timelines, coordinate reviewer assignments, and ensure documentation is complete and compliant. Strong CRO/pharma experience and attention to detail are essential.

Formación

• BSc Life Science degree with CRO/pharma experience.
• Strong written and verbal communication skills.
• Experience with one or more data management systems (e.g., Rave).
• Excellent time management and prioritization abilities.

Responsabilidades

• Create and maintain Study Trackers.
• Monitor screening deadlines and escalate data entry issues.
• Review study visits for readiness of CR review.
• Create and process assignments to reviewers, including query tracking.
• Compile files for patient profile creation and post on Central Grading Portal.
• Prepare CRS agenda and meeting minutes for distribution.
• Maintain action/decision logs and filing on eTMF.
• Collaborate with Directors, Therapeutic Experts, team members and Sponsors.
• Support CRS data review processes and timelines.

Conocimientos

Written communication

Verbal communication

Time management

Attention to detail

Educación

BSc Life Science

Herramientas

Rave

Descripción del empleo

ICON Strategic Solutions is seeking a Central Review Coordinator to join the Central Review Services team. The role supports centralized endpoint data evaluation and data management for a major sponsor in a CRO setting.

The successful candidate will manage trackers, monitor timelines, coordinate reviewer assignments, and ensure documentation is complete and compliant. Strong CRO/pharma experience and attention to detail are essential.