Lead Data Manager (Sponsor Dedicated)

Pharmaceutical Research Associates, Inc; South Africa; Remote; ZAR 40 000 - 80 000; Full time

Job summary

Join a leading global clinical research organization as a Lead Global Data Manager, where you will oversee data management activities across clinical trials. This role involves ensuring data integrity, coordinating with internal teams and external stakeholders, and maintaining high standards of quality and compliance. You will have the opportunity to lead projects, manage vendor relationships, and contribute to a diverse and inclusive workplace. This innovative firm offers a range of benefits to support your well-being and career development, making it an exciting opportunity for those passionate about clinical research.

Benefits

Health insurance options

Retirement plans

Global Employee Assistance Programme

Life assurance

Childcare vouchers

Gym memberships

Qualifications

• Experience in clinical research and data management.
• Ability to work in diverse, cross-functional teams.

Responsibilities

• Oversee and coordinate Data Management activities across clinical trials.
• Ensure data integrity and quality through oversight controls.

Skills

Data Management

Project Management

Microsoft Office

Data Analysis

Communication Skills

Education

Bachelor’s degree in Health or Science

Job description

Overview

As a Lead Global Data Manager, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.

Responsibilities

You will oversee and coordinate Data Management activities across one or more clinical trials. Develop and maintain successful working relationships with internal teams and external stakeholders to ensure data integrity and quality.

Services rendered will adhere to applicable client SOPs, WIs, policies, local regulatory requirements, etc.

What you will be doing:

• Provide data management support, oversight, and accountability for clinical trials.
• Lead with trial customers and partners to establish and confirm data management expectations.
• Gather requirements for eCRF and data collection tools; establish conventions and quality expectations; set timelines and follow up on milestones.
• Perform trial level oversight controls as described in oversight plans and QC processes.
• Create clinical data management documents ensuring quality, compliance, and clarity.
• Ensure real-time inspection readiness of Data Management deliverables and participate in audits.
• Plan, create, and track data management deliverables such as CRFs, review plans, QC plans, datasets, and submission packages.
• Participate in clinical working groups to align Data Management with trial needs.
• Identify lessons learned and best practices; present and train at meetings as needed.

Qualifications

You possess:

• Bachelor’s degree in Health or Science with clinical research experience.
• Data Management experience, required for base and advanced levels.
• Experience working on clinical trials and in diverse, cross-functional, global teams.
• Project and vendor management skills.
• Advanced skills in Microsoft Office, data analysis, and interpretation.
• Excellent organization, communication, and presentation skills.

What ICON can offer you:

We prioritize building a diverse culture that rewards high performance and nurtures talent. Our benefits include:

• Various leave entitlements
• Health insurance options
• Retirement plans
• Global Employee Assistance Programme
• Life assurance
• Optional benefits like childcare vouchers, gym memberships, and more.

Visit our careers website for more: https://careers.iconplc.com/benefits

ICON is committed to inclusion and providing an accessible environment. We encourage all qualified applicants to apply. For accommodations, please contact us via the provided link.

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