Senior Clinical Data Science Lead - (Client Dedicated)

Pharmaceutical Research Associates, Inc; South Africa; Remote; ZAR 800,000 - 1,200,000; Full time

Job summary

A leading global clinical research organization is seeking a Senior Clinical Data Science Lead in South Africa. The successful candidate will be responsible for leading data review activities in clinical trials and providing insights into clinical systems. This is an opportunity to join a diverse and inclusive company that values high performance and well-being.

Benefits

Competitive salary

Comprehensive benefits

Well-being initiatives

Work-life balance opportunities

Qualifications

• Requires strong experience in clinical data management, ideally leading DM for at least 5 studies.
• Good knowledge of clinical data activities including data review and risk management.
• Engaging, supportive leader with a degree in a scientific or healthcare field.

Responsibilities

• Lead end-to-end data review activities performed on clinical trials.
• Serve as primary point of contact for internal/external teams on data review.
• Provide input into clinical system development and clinical risk management.

Skills

Data review

Risk management

Analytics

Clinical systems

Clinical data management

Education

Degree in a relevant Scientific or Healthcare discipline

Tools

Rave

Veeva EDC

Inform

Job description

Overview

As a Senior Clinical Data Science Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Working within one of our newest partnerships you will be embedded in a global company that has relentlessly followed the science to find solutions for patients with critical unmet medical needs. On this top pharma partner, you'll be able to extend and deepen on the knowledge and understanding of cellular oncogenic pathways and immune system function, to advance on research across Oncology and Inflammation & Autoimmunity.

Responsibilities

What you will be doing:

• Lead end to end data review activities performed on a clinical trial. Accountable for achieving clinical data science deliverables on-time, with high- quality and to agreed financial metrics.
• Serve as primary point of contact for internal and external team members regarding clinical data review activities and leads these data review activities to ensure delivery of data fit for analysis.
• Provides input into clinical system development activities and clinical risk management activities.

Qualifications

You are:

• Degree qualified in a relevant Scientific or Healthcare discipline.
• Good knowledge of clinical data science activities (Data review, risk management & analytics, clinical systems).
• Strong experienced in clinical data management. Ideally having been the lead DM for at least 5 studies in start up and 5 database locks.
• DM experience in the CRO industry is preferred.
• Engaging, supportive and you lead by example.
• Experience with Rave and Veeva EDC preferred, Inform desirable.

What ICON can offer you:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodationsInterested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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