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    ME

    Medac

    Pharmaceuticals

    Medical Expert - Clinical Science (all genders)

    Headquarter - Wedel, GermanyHybridFull-timePosted 3mo ago
    All Medac jobs

    Job description

    About the Role

    Leads and evaluates medac’s Managed Access Programs (MAP) and Named Patient Use (NPU) requests from a clinical and ethical perspective, ensuring robust benefit–risk assessments and patient-focused decision-making.
    Hands-on Medical Expert responsible for executing clinical-scientific activities across the product lifecycle, focussed on the development of high-quality regulatory documentation (CTD) and support of global submissions and lifecycle management.
    Acts as a cross-functional clinical partner, translating clinical data into consistent scientific messaging and supporting decision-making across Clinical Science. Brings experience in innovative therapies, including cell therapies, within evolving clinical and regulatory environments.

    Key Responsibilities

    • Lead and evaluate medac’s Managed Access Programme and Named Patient Use (NPU) requests from a clinical and ethical perspective

    • Ensure robust benefit–risk justification, regulatory alignment and high-quality documentation

    • Interface with regulatory, legal, Pharmacovigilance and commercial stakeholders on access strategies

    • Author, review and lead high-quality clinical and regulatory documents (CTD), including Clinical Overview & Clinical Summary, Clinical Expert Statements, Risk Management Plans (RMPs), SmPC, CCDS, PIL, PSURs / DSURs and other Lifecycle documents

    • Ensure scientific consistency, quality across submissions and lifecycle documentation, including for complex products such as cell therapies / ATMPs

    • Contribute to regulatory strategy documents, briefing packages and support global regulatory interactions, including scientific advice procedures and Health Authority meetings

    Your Profile

    • Medical Doctor required

    • Deep understanding of global drug development and regulatory frameworks

    • Strong background in Phase I-III trials, medical monitoring and clinical practice

    • Demonstrated experience in cell therapies /ATMPs (highly preferred), Managed Access Programs/Named Patient Use, Regulatory submission (CTD authoring, Module 2)

    • Therapeutic expertise in oncology, hematology, rheumatology or immunology

    • Exceptional storytelling capability

    • Strong analytical thinking and benefit-risk assessment skills

    • Ability to translate complex science into clear strategic recommendations

    • Language: Fluent English, some German preferred

    Our employees are our greatest asset. And to show our appreciation, we offer attractive benefits:

    • Your work-life balance is important to us. We offer flexible working hours with the option of working a proportion of those hours remotely, 30 annual vacation days and an excellent cafeteria

    • Attractive salaries and success-based bonuses for all medac employees

    • Individual training opportunities: Our medac academy offers a wide range of programmes including leadership training, coaching essentials and language classes

    • A funded pension scheme and other social benefits

    • We care for our employees beyond the workplace and provide advice on caring for elderly relatives as well as offering counselling

    • We promote sports and activities to improve our employees’ health

    Job details are sourced from the employer's original posting.

    Open job posting
    ME

    About the company

    Medac

    Medac is a company operating in the fields of immunology and oncology.

    View all Medac jobs
    Industry
    Pharmaceuticals
    Open roles
    27

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