Lead Clinical Data Manager for Global Trials (Remote)

Sa Metal Group

Cape Town

Remote

ZAR 1,000,000 - 1,200,000

Full time

3 days ago
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Benefits offered by this job

Fully remote
Company equipment provided
Competitive salary
Career growth opportunities

Job summary

IQVIA is hiring experienced Clinical Data Management Leads to oversee end-to-end data management for global clinical trials. You'll ensure quality, compliance, and timely delivery while guiding cross‑functional teams in a remote work setting with all necessary equipment provided.

Ideal candidates hold a life sciences degree, 10+ years in CDM with 5+ years in a lead role, and hands‑on experience with Medidata Rave or Oracle InForm, plus strong knowledge of GCP/ICH and leadership.

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 CDM role.
  • Experience managing large global studies (1000+ patients).
  • Proficiency with Medidata Rave, Oracle InForm or similar EDC systems.
  • Strong understanding of GCP, ICH, and clinical research processes.

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

Clinical Data Management
Lead Data Management
Regulatory Compliance
Project Management
Medidata Rave
Oracle InForm
GCP/ICH Knowledge
Team Leadership
Communication

Education

Bachelor's degree in life sciences, health, clinical, biological, or mathematical field

Tools

Medidata Rave
Oracle InForm

Job description

IQVIA is hiring experienced Clinical Data Management Leads to oversee end-to-end data management for global clinical trials. You'll ensure quality, compliance, and timely delivery while guiding cross‑functional teams in a remote work setting with all necessary equipment provided.

Ideal candidates hold a life sciences degree, 10+ years in CDM with 5+ years in a lead role, and hands‑on experience with Medidata Rave or Oracle InForm, plus strong knowledge of GCP/ICH and leadership.

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