Senior Global Clinical Trial Lead

4 days ago


Centurion, South Africa IQVIA Full time

A global leader in clinical research services is seeking a Clinical Trial Manager in Centurion, South Africa. The successful candidate will lead clinical teams, ensure compliance with regulations, and manage project finances. Applicants must have a Bachelor's degree in health care or a scientific discipline and at least 2 years of clinical trial management experience. This role contributes to bringing new medical treatments to market faster.#J-18808-Ljbffr



  • Centurion, South Africa IQVIA Biotech Full time

    A leading global clinical research organization is seeking a Clinical Trial Manager in Centurion, South Africa. The role requires oncology experience and involves ensuring compliance with regulations, managing project finances, and leading clinical teams. Candidates must have a Bachelor's degree in healthcare or a related scientific discipline and a minimum...


  • Centurion, Gauteng, South Africa IQVIA Full time R800 000 - R1 200 000 per year

    Clinical Trial Manager - IQVIA Biotech * Please note: due to sponsor requirements for the role only candidates based in the listed location/s and with previous Global CTM experience will be considered. Any applications from candidates based outside of these locations will not be considered.Job OverviewClinical Trial Managers (CTM) are an integral part of...


  • Centurion, South Africa Novasyte Full time

    Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...


  • Centurion, South Africa IQVIA Biotech Full time

    Overview Clinical Trial Manager - IQVIA Biotech Oncology experience required. Responsibilities Ensure clinical delivery of assigned projects in compliance with regulatory requirements (ICH-GCP protocol), customer requirements (contract), and internal requirements (policies SOPs). Accountable for meeting project recruitment targets and ensuring appropriate...


  • Centurion, South Africa IQVIA Full time

    **ASSIGNMENT PROFILE** **Clinical Trial Coordinator (CTC)** **Description of Roles and Responsibilities** - **Trial and site administration**: - Tracking (e.g. essential documents) and reporting (e.g. Safety Reports) - Ensure collation and distribution of study tools and documents - Update clinical trial databases (CTMS) and trackers - Clinical supply &...


  • Centurion, South Africa IQVIA Full time

    Clinical Trial Manager - IQVIA Biotech * Please note: due to sponsor requirements for the role only candidates based in the listed location/s and with previous Global CTM experience will be considered. Any applications from candidates based outside of these locations will not be considered. Job Overview Clinical Trial Managers (CTM) are an integral part of...


  • Centurion, South Africa IQVIA Full time

    **For GCO**: Services/deliverables include the management of all documents and logístical and administrative tasks related to trial feasibility, start-up, execution and close out of clinical trials. Ensures trial related activities are compliant with GCO SOPs, policies, code of Good Clinical Practice (GCP), Health Care Compliance requirements (HCC) and...


  • Centurion, South Africa IQVIA LLC Full time

    A prominent clinical research organization in Centurion is seeking an experienced Project Lead to oversee clinical studies. Responsibilities include leading project teams, ensuring compliance with clinical regulations, and fostering collaboration across departments. The ideal candidate will have a Bachelor's Degree in Life Sciences and at least 5 years of...


  • Centurion, South Africa IQVIA Full time

    **Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. - Assist the clinical team with the preparation, handling, distribution,...


  • Centurion, South Africa Labcorp Full time

    Labcorp is looking to recruit a SCTA (CTC) to join our sponsor in South Africa! **Responsibilities**: **TRIAL AND SITE ADMINISTRATION**: - Tracking (e.g. essential documents) and reporting (e.g. Safety Reports) - Ensure collation and distribution of study tools and documents o Update clinical trial databases (CTMS) and trackers - Clinical supply &...