Remote Central Review Coordinator - Data-Driven Safety

Placements24; East London; A distancia; ZAR 420.000 - 660.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global EAP LifeWorks

Life assurance

Descripción de la vacante

ICON Strategic Solutions is seeking a Central Review Coordinator to join the Central Review Services team. You will manage data review processes, track study activities, and ensure timely delivery for one or more sponsor projects.

The role emphasizes collaboration with Directors, Sponsors, and cross-functional teams, with a focus on accuracy, timelines, and compliance in centralized endpoint data evaluation.

Formación

• BSc Life Science degree completed.
• Experience in CRO/pharma industry.
• Knowledge of data management systems and study tasks.

Responsabilidades

• Create and maintain Study Trackers.
• Monitor screening deadlines; follow up with sites on data entry and queries.
• Review study visits and sweeps for readiness for review.
• Create, send and process reviewer assignments; track queries.
• Download and compile files for patient profile creation and CRS posting.
• Prepare CRS agenda and distribute meeting minutes.
• Update action/decision logs and file documents in Central Grading Portal.
• Liaise with Directors, Therapeutic Experts, internal teams and Sponsors.
• Perform reviews of study datasets prior to client transfer when applicable.
• Monitor progress to meet timelines; identify issues and report to Lead Central Review Manager.
• Participate in database lock activities.
• Serve as CR Coordinator on one or more projects.

Conocimientos

Data management

Cross-functional teamwork

Excellent communication

MS Word & Excel

Attention to detail

Time management

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. You will manage data review processes, track study activities, and ensure timely delivery for one or more sponsor projects.

The role emphasizes collaboration with Directors, Sponsors, and cross-functional teams, with a focus on accuracy, timelines, and compliance in centralized endpoint data evaluation.