Clinical Data Management Lead at The IQVIA, Apply now!

Full-time
  • Full-time
  • Centurion, Gauteng
  • Market Related ZAR / Month
  • Salary: Market Related

IQVIA

Job Details

πŸ“Œ Job Title: Clinical Data Management Lead
🏒 Company: IQVIA
πŸ“ Location: Centurion, Gauteng, South Africa (Home-Based)
πŸ•’ Employment Type: Full-Time
🏠 Work Setup: Remote / Home-Based
πŸ†” Job ID: R1540796
πŸ’Ό Industry: Clinical Research / Life Sciences


Company Overview

IQVIA is a global leader in clinical research, healthcare analytics, and life sciences solutions. The company leverages advanced data science, technology, and domain expertise to accelerate the development and commercialization of innovative medical treatments, improving patient outcomes worldwide.


Job Overview

IQVIA is seeking a Clinical Data Management (CDM) Lead to oversee data management activities across large-scale global clinical trials. This role involves leading multiple studies, managing stakeholder relationships, and ensuring high-quality data delivery throughout the clinical development lifecycle.

The successful candidate will act as a subject matter expert, providing technical leadership, driving process improvements, and ensuring compliance with regulatory standards.


Key Responsibilities

  • Serve as the primary point of contact for clients on data management deliverables
  • Manage multiple global clinical trials or programmes simultaneously
  • Provide leadership and guidance to Data Team Leads (DTLs)
  • Lead project management activities including timelines, resources, and deliverables
  • Conduct client negotiations on budgets, timelines, and processes
  • Ensure quality and timely delivery of data management outputs
  • Act as escalation point for complex data issues
  • Develop, review, and approve Data Management Plans (DMPs)
  • Monitor service performance and implement continuous improvement initiatives
  • Provide subject matter expertise in clinical data management processes
  • Lead best practice initiatives and contribute to SOP development
  • Manage budgets and scope of work (SOW) independently

Qualifications

Education

  • Bachelor’s Degree in Health Sciences, Clinical, Biological, Mathematical Sciences, or related field

Experience

  • Approximately 7+ years of Clinical Data Management experience
  • At least 5 years as a CDM Project Lead
  • Experience managing large global trials (1000+ patients)
  • Proven experience in stakeholder engagement and client negotiations

Skills

  • Advanced knowledge of clinical data management processes
  • Understanding of Good Clinical Practice (GCP) and regulatory requirements
  • Knowledge of pharmacology, anatomy, and medical terminology
  • Strong project management and organisational skills
  • Excellent communication and stakeholder management abilities
  • Problem-solving and analytical thinking
  • Ability to work independently in a remote environment

CV Tips

  • Highlight your clinical trial experience, including scale and therapeutic areas
  • Showcase leadership roles in data management projects
  • Include experience with global trials and regulatory compliance (GCP)
  • Demonstrate stakeholder management and client interaction experience
  • Provide measurable outcomes (e.g., improved data quality, reduced timelines)
  • Structure your CV: Summary β†’ Clinical Projects β†’ Leadership Experience β†’ Achievements β†’ Skills

Benefits of Joining the Company

  • Work with a global leader in clinical research and healthcare innovation
  • Fully remote role offering flexibility and work-life balance
  • Exposure to international clinical trials and cutting-edge research
  • Opportunities for career growth and leadership development
  • Collaborative and diverse global work environment

Company Policy

IQVIA maintains a strict commitment to integrity and ethical hiring practices. All candidate information must be accurate and truthful, as any misrepresentation may result in disqualification or termination. The company promotes equal opportunity employment and values diversity, ensuring fair consideration for all qualified applicants.

To apply for this job please visit jobs.iqvia.com.