PAREXEL Recruitment

About PAREXEL

PAREXEL Jobs in South Africa

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  • • Contract Clinical Research Associate (CRA - Independent Consultant) at PAREXEL

    • Essential Knowledge and Experience Required: Substantial Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and termin
    • • 28 October, 2024
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  • • Contracts Specialist at PAREXEL

    • About this Role External Job Description We are now looking for a Contracts Specialist. In this role, you will amend, negotiate and finalise project budgets together with creating draft contrac
    • • 25 September, 2024
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  • • Medical Director - Infectious Disease at PAREXEL

    • About this Role Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scien
    • • 25 September, 2024
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  • • Senior Medical Director - Pharmacovigilance/Drug Safety at PAREXEL

    • Job Purpose The Senior Medical Director is responsible for providing leadership and directions to the Safety Medical Sciences business functions and other assigned business functions, as well as
    • • 25 September, 2024
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  • • Global Site Contracts Lead at PAREXEL

    • About this Role Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scien
    • • 25 September, 2024
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  • • Biometrics Delivery Lead at PAREXEL

    • About This Role Role is remote - it can be based in select EMEA locations. Picture Yourself At Parexel: The Biometrics Delivery Lead (DL), reporting into the Global Biometrics Account Lead (
    • • 25 September, 2024
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  • • Senior Regulatory Affairs Associate - CTA at PAREXEL

    • About This Role We are looking for a Senior Regulatory Affairs Associate with working knowledge of Clinical Trial Applications (CTA) to join our team in South Africa! This role can be office bas
    • • 25 September, 2024
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  • • Senior Statistical Programmer / Statistical Programmer II at PAREXEL

    • About This Role The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific areas providing technical
    • • 25 September, 2024
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  • • Senior Biostatistician at PAREXEL

    • About This Role As an experienced Biostatistician, you will lead research design and analytical strategies, provide input into protocols, develop and review statistical analysis plans and author
    • • 25 September, 2024
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  • • Contracts Specialist at PAREXEL

    • About this Role We are now looking for a Contracts Specialist. In this role, you will amend, negotiate and finalise project budgets together with creating draft contractual documents.&nbs
    • • 01 August, 2024
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  • • Senior Regulatory Affairs Associate - CTA at PAREXEL

    • Key Deliverables in the role: Manage the local submissions (as Local Regulatory Contact - LRC) Coordinate the regulatory submissions in all participating countries as Regulatory Lead. Regula
    • • 30 July, 2024
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  • • (Senior) Medical Director, Gastrointestinal at PAREXEL

    • KEY ACCOUNTABILITIES: Project Execution: Medical Monitoring Delivery & PV Support Independently deliver all medical support required for successful delivery of the projects according to c
    • • 30 July, 2024
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  • • Senior Clinical Research Associate at PAREXEL

    • ABOUT THIS ROLE The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-ou
    • • 10 July, 2024
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  • • Senior Medical Writer - Bloemfontein at PAREXEL

    • Key Accountabilities: Author Clinical Documents Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize clinical documents for submission to regulatory aut
    • • 29 April, 2024
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  • • Regulatory Affairs Associate - Clinical Trail Applications (CTA) at PAREXEL

    • Key Deliverables in the role: Manage the local submissions (as Local Regulatory Contact - LRC) but should also be able to coordinate the regulatory submissions in all participating countries as
    • • 29 April, 2024
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  • • Intern – Statistical programmer at PAREXEL

    • You will support Statistical Programming group in analyzing and reporting clinical trials. Your tasks include: Producing datasets (for statistical analysis and regulatory submission purposes), s
    • • 29 April, 2024
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  • • Business Analyst at PAREXEL

    • Your key responsibilities will include, but are not limited to: Taking responsibility for investigative work to determine business requirements and specify effective business processes, practice
    • • 03 April, 2024
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  • • Controlled Document Specialist I at PAREXEL

    • Summary of this Position: Support the development, analyzes, documentation, and continuous improvement of controlled processes withing the company, as per current formats/standards which is a key c
    • • 15 March, 2024

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