Clinical Trial Manager

2 weeks ago

Johannesburg, Gauteng, South Africa Icon Full time
At ICON, it's our people that set us apart.

Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.


Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity.

We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point.

In short, to be the partner of choice in drug development.

That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us.

You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.


About ICON's IEB Solutions Team:

ICON's global Early Clinical & Bioanalytical (IEB) Solutions team includes six clinical research units and three bioanalytical labs, in addition to dedicated early phase projects and data & scientific services.

IEB specializes in delivering solution-focused support for our customers' Phase I-IIa healthy and early patient trials.

The Role:
The Clinical Trial Manager in IEB is responsible for the delivery of all clinical aspects of the study.

The CTM oversees the clinical portion of the budget, develops monitoring plans & tools, trains CRAs, drives enrollment and study start-up activities, reviews trip reports, implements corrective and preventative action plans, liaises with the Sponsor, vendors & cross-functional teams, identifies & mitigates risks that may impact clinical delivery, and provides reporting & metrics on all clinical activities.

The CTM will also participate in Sponsor, Investigator, and bid defense meetings.

You Will Need:
Degree in a Life Sciences or related disciplineDemonstrated ability to drive the clinical deliverables of a studySubject matter expertise in the designated therapeutic areaPrior monitoring experience is preferredUnderstanding of early phase studiesAbility to travel up to 20%Fluency in English - both written & verbal

Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.

We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.

But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.


ICON is an equal opportunity and inclusive employer and 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.

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