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  • Posted: Nov 25, 2020
    Deadline: Not specified
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    With 46 years’ experience in successful job-matching and placement of top candidates, Kelly - a division of Kelly Group - forms a part of Adcorp Holdings Limited (listed on the JSE in 1987), ), South Africa’s leading provider of staffing, human capital management and business process outsourcing services, we have access to financial resources, le...
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    Clinical Trial Project Leader (Pharmaceuticals)


    We're seeking a Clinical Trial Project Leader (Pharmaceuticals) – Midrand to be responsible for allocated clinical trials/studies within the cluster, ensuring compliance with the companies quality standards and processes, regulations in force, the forecasted

    Duties & Responsibilities

    •  Overall responsible and accountable for allocated clinical trials within the Clinical Study Unit.
    •  All study related activities at various stages of a clinical study – start up, recruitment, maintenance,close out and archiving.
    • Study activities performed according to Good Clinical Practice, regulations in force and company standards and processes.
    • Supports the management team in driving the Clinical Study Unit       
    • Primary contact with identified key stakeholders - Ensures appropriate communication and support with these stakeholders.
    • Selection of clinical trial sites.
    • Submissions to Ethics Committees / IRBs
    • Training of sponsor and clinical trial personnel on study related processes and requirements.
    • Contract negotiation and agreement with Clinical Trial sites.
    • Maintaining clinical study documentation in an audit ready state.
    • Compliance with requirements to all study related databases.
    • High quality standards of study data collection and prompt data query resolution.
    • Adequate provisioning of study materials and devices.
    • Oversee monitoring activities through regular contacts with local monitoring team, local teammeetings, review of monitoring visit reports and adherence to the monitoing plan.
    • Preparation and prompt responses to audit/inspection reports and implementation of recommendations.

    Desired Experience & Qualification

    • University degree in Health Sciences or equivalent
    • Clinical Research experience essential, minimum 5 years
    • Knowledge of GCP/ICH phase I-IV clinical trials
    • Computer skills must include working knowledge of Excel, PowerPoint,
    • Word and Outlook
    • Project and people management skills
    • Organizational, analytical and planning abilities
    • Fluent in English
    • Literate in French will be an advantage

    Package & Remuneration

    • Permanent
    • Market Related 

    Method of Application


    • Email your CV to .
    • N.B. If you're emailing us directly, remember to insert : "Clinical Trial Project Leader (Pharmaceuticals) – Midrand" in the email subject line, for consideration

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