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ICON plc Recruitment

About ICON plc

We offer a full range of consulting, clinical development and commercialisation services from a global network of offices in 46 countries Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives an... read mored improve quality of life. We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients reducing time to market, reducing cost and increasing quality and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the worlds leading Contract Research Organisations through a number of high-profile industry awards.

ICON plc Jobs in South Africa

86 vacancies
      • Study Start Up Associate at ICON plc

      • What You Will Do: Your role will involve delivering site start-up and activation work to a high standard, working closely with your team and stakeholders. Key responsibilities include:
        • 27 October
      • Senior Clinical Research Associate at ICON plc

      • What You Will Do: You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: Monitor
        • 27 October
      • AI Engineer at ICON plc

      • As an AI Engineer at ICON, you will develop and implement programming solutions that enhance the analysis of clinical trial data. What You Will Do: You will take responsibility for clini
        • 27 October
      • Statistical Programmer at ICON plc

      • As a Statistical Programmer at ICON, you will the development, validation, and execution of statistical programs to support clinical trial analysis and reporting. You will be working with as part o
        • 27 October
      • Senior Clinical Trial Manager - Biotech at ICON plc

      • We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc - this position will sit within ICON Biotech. In this critical role, you will be responsible for o
        • 07 October
      • Senior Clinical Research Associate at ICON plc

      • As a SCRA  or CRA at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What Y
        • 07 October
      • Clinical Trial SME at ICON plc

      • Firecrest Clinical is part of the ICON plc Group and produces highly visual and engaging products for the Clinical Trial Industry. Firecrest products help improve Site performance by delivering inn
        • 07 October
      • Senior Clinical System Lead at ICON plc

      • As a Senior Clinical System Lead at ICON, you will play a critical role in the successful delivery of clinical trial systems that support global clinical research programmes. Acting as the lead sys
        • 07 October
      • Senior Site Activation Lead at ICON plc

      • The Role: Our industry leading Global Study Start Up group is growing and we are  currently looking for Senior Site Activation Leads to join our evolving global team.  This i
        • 15 December, 2024
      • CTA at ICON plc

      • As a CTA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The Global Clinical Study Coordinator MAO, ass
        • 15 December, 2024
      • Clinical Trial Manager at ICON plc

      • What you will be doing: Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality. Leads Local Study Team consisting of CR
        • 15 December, 2024
      • Senior Biostatistician II at ICON plc

      • What You Will Be Doing: Designing and implementing statistical analyses for clinical trials, including the development of statistical analysis plans and interpretation of results. Collaboratin
        • 15 December, 2024
      • Director, Regulatory Operations at ICON plc

      • What you will be doing Lead and oversee regulatory operations activities to ensure compliance with applicable regulations and guidelines. Develop strategies for regulatory submissions and app
        • 15 November, 2024
      • Statistical Programmer II at ICON plc

      • As a Statistical Programmer II you will be responsible for statistical aspects of clinical and preclinical research projects. Project responsibilities include study design, case report form develop
        • 15 November, 2024
      • Manager, Quality Assurance at ICON plc

      • What you will be doing: Developing and implementing quality assurance strategies and processes to support clinical trial activities. Conducting quality assessments and audits to ensure complia
        • 15 November, 2024
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