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  • Posted: Sep 24, 2025
    Deadline: Not specified
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  • Mango5 is one of the top BPO Outsource Centres in South Africa, offering outsourced services to local and international clients. Our Contact Centre in Cape Town has a rich history of delivering best in class BPO services. Mango5 has built a reputation of delivering quality outsourced service offerings since December 2005. Our product offerings have always...
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    Team Manager

    Key Responsibilities:

    • Lead, supervise, and motivate a team of Junior Clinical Data Coordinators.
    • Monitor performance and provide coaching to achieve targets
    • .Ensure compliance with client policies and quality standards.
    • Resolve escalated issues and support complex recruitment cases.
    • Prepare and present detailed performance reports.
    • Foster a collaborative and positive team culture.
    • Identify and implement process improvements.
    • Maintain clear communication with clients and stakeholders.

    Skills and Experience:

    • 3-4 years of leadership experience in healthcare, recruitment, or call centre settings.
    • Proven ability to manage and develop high-performing teams
    • Familiarity with medical terminology, treatment procedures, and industry regulations to enhance communication and understanding with potential patients
    • Do you have a high school diploma or equivalent qualification
    • Strong problem-solving and conflict-resolution skills.
    • Proficiency in CRM platforms, reporting tools, and Microsoft Office.
    • Excellent communication and interpersonal skills.
    • Knowledge of compliance and regulatory standards in recruitment and healthcare.

    go to method of application »

    Junior Clinical Data Coordinator

    Key Responsibilities

    • Manage incoming clinical research data across multiple worksheets, systems, and image files.
    • Ensure accurate data entry and escalate issues appropriately.
    • Apply critical thinking and discretion, particularly in relation to adverse events.
    • Upload visit data within defined timelines.
    • Review project data and deliver results to stakeholders promptly.
    • Request and manage source data corrections as required.
    • Enter/upload data into third-party platforms (e.g., EDC systems).
    • Review and resolve data queries.
    • Participate in database lock activities.
    • Conduct regular quality checks of data for completeness, accuracy, and integrity (ALCOA+).
    • Assist in the identification and reporting of potential adverse events.
    • Maintain project documentation and the Trial Master File (TMF).
    • Assist in the creation and maintenance of case report forms.

    Qualifications:

    • Matric certificate (minimum requirement).
    • Bachelor’s degree in a life sciences-related field (Advantagouss).
    • 1–2 years of clinical trial and data management experience.
    • Knowledge of Good Clinical Practices (GCP).
    • Experience with electronic data capture (EDC) systems (preferred).
    • Strong skills in the use of technology, tools, operating systems, and software.
    • Strong organizational skills with experience balancing priorities and resources.
    • Strong attention to detail.
    • Critical thinking and problem-solving skills.
    • Ability to plan proactively, anticipate challenges, and operationalize solutions.
    • Able to work thoughtfully and decisively, fostering an inclusive work environment.
    • Clear criminal record.
    • Clear credit record.

    Method of Application

    Use the link(s) below to apply on company website.

     

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