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    Clinical Scientific Program Lead (m/f/d)

    from: 27.09.2022
    medac is a dynamic company that has been growing continuously for over fifty years. More than 2,000 employees work on the further development of medical products and medical devices for the diagnosis and treatment of oncological, urological and autoimmune diseases. We are one of the leading pharmaceutical companies, in particular in the field of niche products.
    • Acts as global clinical program lead, overseeing multiple trials in a clinical development program
    • Leads the clinical program team being accountable for excellence in clinical trial strategy and leadership for design, execution and reporting ensuring high quality data
    • Supervises the planning and proactive management of clinical program(s)
    • Undertakes product and therapeutic area reviews and provides evidence-based medical and scientific input to trial-related, strategic and regulatory documents
    • Is accountable for delivering the medical aspects of the clinical development plans and TPPs
    • Contributes to the core medical/scientific information required in all clinical documents (e.g. study protocols, clinical trial reports, safety related documents) and assures preparation of high quality documents
    • Contributes to development of publication plans in collaboration with other internal departments
    • Provides clinical and scientific oversight for assigned clinical development programs, including medical monitoring across multiple clinical trials in collobaration with qualified in- or external persons
    • Supports the evaluation of potential clinical development projects for in- or out licensing purposes and other departments with clinical and scientific input, if required
    • University Degree in Lifescience required, Medical Degree preferred
    • At least 5 years’ international experience in Clinical Research Phase I-III
    • Highly productive and well organized regulatory writer
    • Experience in strategic planning, executing and designing of Clinical Development Plans and trial protocols
    • Experience with regulatory interactions gained during previous submissions to EMA, FDA or PMDA
    • Firm knowledge of GCP/ICH rules and relevant laws and regulations
    • Team player with strong communication skills
    • Excellent analytical skills combined with a strategic vision
    • Language: Fluent English, some German preferred

    • Your work-life balance is important to us. We offer flexible working conditions with the option of working up to 60% of your 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 and childcare
    • We promote sports and activities to improve our employees’ health
    If you are looking for a new career challenge and a future-oriented role, then we are looking forward to receiving your application including your earliest possible starting date and salary expectations. For your convenience, please feel free to use our online application form on
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