Remote Data Management Lead for Global Clinical Trials

IQVIA LLC

Bloemfontein

On-site

ZAR 1,000,000 - 1,350,000

Full time

14 days+
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Benefits offered by this job

Fully remote role
Competitive salary
Career growth opportunities
Global collaboration

Job summary

IQVIA LLC is seeking an experienced Clinical Data Management Lead to oversee end-to-end data management for global clinical trials in a remote/WFH setup. You will ensure quality, accuracy, and regulatory compliance while leading cross-functional teams to bring new therapies to life.

The role requires 10+ years in CDM with 5+ years in a lead capacity, expertise in Medidata Rave/Oracle InForm, and strong GCP/ICH knowledge. Expect collaboration with global teams and opportunities for career growth.

Qualifications

  • Bachelor’s degree in life sciences, health, clinical, biological, or mathematical field.
  • At least 10 years of direct clinical data management experience with 5+ years in a Lead role.
  • Experience leading global studies (1000+ patients) preferred.
  • Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.
  • Strong knowledge of GCP/ICH and clinical research processes.
  • Excellent communication and leadership skills.

Responsibilities

  • Lead data management for complex, global clinical trials from study setup to database lock.
  • Serve as the main client contact for all 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

CDM Leadership
Cross-functional leadership
EDC systems
GCP/ICH knowledge
Communication
Project management
Medidata Rave

Education

Bachelor’s degree in life sciences or related

Tools

Oracle InForm
Medidata Rave

Job description

IQVIA LLC is seeking an experienced Clinical Data Management Lead to oversee end-to-end data management for global clinical trials in a remote/WFH setup. You will ensure quality, accuracy, and regulatory compliance while leading cross-functional teams to bring new therapies to life.

The role requires 10+ years in CDM with 5+ years in a lead capacity, expertise in Medidata Rave/Oracle InForm, and strong GCP/ICH knowledge. Expect collaboration with global teams and opportunities for career growth.

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