Executive Assistant: Global Travel & Events

Luno; Cape Town; Remote; ZAR 900,000 - 1,300,000; Full time

Benefits offered by this job

Fully remote role - company equipment

Competitive salary and performance‑in‑

Career growth and mentoring

Inclusive, global culture

Job summary

IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life.

This is a remote/WFH position with all necessary equipment provided. What You'll Do includes leading data management for global trials, serving as client contact, and ensuring regulatory compliance.

Qualifications

• Bachelor's degree in life sciences, health, clinical, biological, or mathematical field.
• 10+ years of direct clinical data management experience, with 5+ years in a Lead role.
• Experience with Medidata Rave or Oracle InForm.
• Strong knowledge of GCP, ICH, and clinical research processes.
• Excellent communication and leadership skills.

Responsibilities

• Lead data management for global clinical trials from study setup to database lock.
• Serve as the main client contact for data management deliverables.
• Oversee SAE, PK, and external data reconciliation and database deployment.
• Manage timelines, budgets, and resource allocation to meet customer expectations.
• Mentor junior data management staff and promote best practices.
• Drive process improvements and ensure regulatory and SOP compliance.

Skills

Leadership

Communication

GCP/ICH knowledge

Education

Bachelor's degree in life sciences or related field

Tools

Medidata Rave

Oracle InForm

Job description

IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life.

This is a remote/WFH position with all necessary equipment provided. What You'll Do includes leading data management for global trials, serving as client contact, and ensuring regulatory compliance.