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  • Posted: Sep 19, 2025
    Deadline: Not specified
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  • Sharing a Vision to Drive Healthcare Forward Healthcare is an industry designed to help humans. As a global community, we continuously invest and commit to advancing human health. To deliver value and real outcomes. To rise to the challenge to find the next breakthrough by making the most of increasingly limited resources. We are inspired by the potential ...
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    Associate Consultant, Market Access Insights

    Job Description

    Real World Commercial Solutions to Create a Healthier World

    • In RWCS we’re passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world.
    • Every day our team develops evidence-based strategies that are used in published research, clinical guidelines, and market access decisions, to improve healthcare at every touchpoint.
    • We design and deliver Commercial Analytics, supported by our world-class proprietary data assets, solve complex client challenges through strategic consulting, and use leading edge market research techniques to support clients brand strategy, planning and measurement.
    • We’re purpose-driven problem solvers, that do what we love to make a greater impact on human health.

    Market Access Insights

    • The mission of the MAI team is to provide our clients with comprehensive and interconnected content which can be accessed flexibly via a variety of options to best suit our client’s needs.

    The options available to our clients include:

    • Online access to an intuitive and easy-to-use platform
    • Data services to facilitate integration of data into in-house systems
    • Client services to support custom projects

    The Role

    • In this role, you’ll be working on projects of varying complexity, from basic analysis and problem-solving to assisting in the development of more complex solutions.
    • This exciting opportunity may allow you to lead small teams or work streams to provide high-quality and on-time input to client solutions for an impact on global projects that drive healthcare forward.

    What You’ll Be Doing

    • Reviewing and analysing client problems and assisting in the development of solutions and detailed documentation
    • Performing quantitative and qualitative analyses of global HTA and reimbursement
    • Conducting competitive intelligence to feed predictive analyses of Regulatory and HTA submissions
    • Assisting in the design, structure, and completion of presentations to the client
    • Proactively developing your knowledge of consulting methodologies and the life sciences market through deliverables and formal and informal learning opportunities

    Who You Are

    • A university degree holder in life sciences with 1-3 years of experience in consulting in Market Access
    • Has experience with global HTA and reimbursement processes
    • A good communicator with excellent interpersonal and team-working skills and strong written, numerical, and problem-solving skills
    • Is able to effectively communicate in verbal and written English
    • Able to adapt, learn quickly, and apply new knowledge
    • An effective team worker with time management skills

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    Senior Data Team Lead

    Job Description Summary

    • Looking out for data management expert, who has prior experience in performing scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS) in the past for at least a duration of 1+ years.
    • Prior experience of closely collaborating with the SRP, SRS, Data Management functions and the rest of the study team members when implementing the data management related activities for protocols, with focus on more complex indication and therapy related elements of the study.
    • Has prior experience of being involved and driving discussions with SRP/SRS and collaborates with the Data management team to establish, align, and confirm scientific clinical data review expectations for assigned trial(s).
    • Extensive prior experience of 4+ years supporting studies within the therapeutic area Oncology or CV&M.

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    Clinical Data Management Lead, FSP, home-based in South Africa

    • You’ll be responsible for managing end-to-end delivery of data management services for multi-service projects, ensuring quality deliverables on time and within budget. You will direct the team in areas of project planning, execution, financial management, communications and milestone deliverables.

    Main responsibilities

    • Provide leadership and vision to the team
    • Manage and deliver several large scale, high complexity/non-standard aspect studies across a range of sponsors and Therapeutic areas
    • Manage sponsors at both Study and Programme Level
    • Manage delivery of areas requiring specific expertise (e.g Process, Finance)
    • Ensure milestones meet timelines and quality deliverables
    • Provide project management expertise working with customer data managers, key decision makers and internal team members to manage continuous process improvements and provide technical expertise
    • Ensure open communications with customer and Quintiles management to manage and meet contractual obligations
    • Provide input for and perform direct negotiations with customer
    • Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders
    • Support DM service delivery with comprehensive DM process and technical expertise in executing projects
    • Create and/or review and sign-off on all data management plan (DMP) documents
    • Track service performance and provide leadership to identify root causes of issues and implement remedial actions
    • Serve as the escalation point for unresolved data issues; work with client data managers, vendors, internal team members for resolution
    • Maintain internal tracking databases and systems

    Minimum Education & Experience

    • Bachelor’s Degree, or educational equivalent, in health, clinical, biological or mathematical sciences, or related field
    • Around 5 years direct Data Management experience, including 3 or more years as a Clinical Data Management project lead is preferred
    • Ability to maintain strong customer relationships

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    Snr Data Strategist

    Job Description

    Minimum Experience

    • Bachelor in Science/Computer Science/Information Technology or Bachelor in Technology with 8 to 10 years’ experience OR equivalent combination of education and experience.
    • At least 7+ years of CRO experience with knowledge of clinical systems, the data points stored within them and data flow paths.

    REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

    • Experience working in Drug Discovery, clinical trial conduct, clinical data management or related industries.
    • Excellent critical thinking and analytical skills, strong attention to detail
    • Effective written, interpersonal, and verbal communication skills
    • Strong influencing, problem resolution, motivation, and negotiation skills
    • Solutionoriented approach to challenges
    • Sound leadership and customer service skills
    • Competent presentation skills meeting the needs of all levels
    • Ability to establish and maintain effective working relationships with team members, management, operations staff, clients, and executive management.
    • Ability to lead effective meetings.
    • Strong organizational and time management skills.
    • Ability to manage multiple dependencies across multiple systems to reach a final deliverable.
    • Ability to establish and maintain effective working relationships with teams involved in study start up.

    RESPONSIBILITIES

    • Work directly with project teams to guide/convey optimal data flow design patterns across the enterprise consisting of multiple systems with the end goal to ensure data integrations enable real time Alerts and Analytics
    • Lead vendor data setup for all Data Management vendors. Work closely with the DTL to enable data flow for all DM downstream activities (data cleaning, etc).
    • Complete and manage the 'Systems Integration Plan' to detail the data flow and highlight potential risks/challenges while collaborating with various groups (i.e. IPA, Study Team, CDAT) to provide data standardization and alignment of site visits across systems”.
    • Champion people, process and technology improvements and standards to enhance quality, increase productivity (internal and external with Investigator sites) and reduce data latency within Quintiles clinical trial systems inclusive of IVxS, EDC, CTMS, QRPM, Data Factory, Triggers and Alerts, Visualizations such as Infosario Analytics and Federated reports, CDOS and SLDRs.
    • Guide and present study teams with best case options given limitations (e.g. contract, cost, timelines, etc.) with the ability to articulate pros and cons of each approach.
    • Identify and implement innovative solutions to challenges and influence future decisionmaking in order to reduce workarounds.
    • Review data transfers specifications to ensure they meet the standards required to develop quality data integrations.
    • Proactively provide education and training to ensure adherence of the relevant startup SOPs and best practices during the RFI and postaward phases.
    • Collaborate with the global IT organization as needed to resolve support issues related to data integration or data quality.
    • Ability holistically understands the process and structure of 510 individual systems and determine how the design of one system may impact the ability of another system to function optimally.

    Method of Application

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