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Senior Central Monitoring Specialist en madrid

Johnson & Johnson

8 - 40 horas por semana

Descripción del empleo


At Janssen, we are dedicated to addressing and solving some of the most important unmet medical needs of our time in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. Driven by our commitment to patients, we bring innovative products, services and solutions to people throughout the world. Janssen is a pharmaceutical company of Johnson & Johnson. Please visit for more information.

Senior Central Monitoring Specialist

Location: Europe or North America

Contract: full time

Janssen Research and Development, L.L.C., a member of Johnson and Johnson's Family of Companies, is recruiting for a Senior Central Monitoring Manager located in Europe or North America including remote based.

At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. We pursue the most promising science, wherever it might be found.

We discover and develop innovative medical solutions to address unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. Visit http://www.JanssenRnD.com to learn more.

The responsibilities & the impact YOU will have:

  • As part of our Risk Management-Central Monitoring team, you will be responsible for executing on the Risk Based Monitoring (RBM) strategy globally within Janssen R&D.
  • You will lead a cross-functional study team through all phases of RBM execution.
  • Some key skill sets include protocol risk assessment, data/risk analysis, technology proficiency and a high degree of leadership and influence skills for translating RBM concepts.

  • Qualifications

    We would love to hear from YOU, if you have:

  • Ability to operate and proactively use various technology systems to analyze risk related to trial quality/performance and compliance and identify trends and early warning signals.
  • Advanced leadership skills including effective communication and the ability to influence across multiple global communication streams
  • Knowledge of ICH-GCP, risk analysis, and overall drug development process
  • Minimum: B.S. degree required. A minimum of three years of clinical trial experience in the pharmaceutical/medical device industry or CRO. Knowledge of basic statistical concepts and data science principles.
  • Preferred: Master’s Degree in Life Sciences. Advanced analytical/statistical skills. Hands-on risk management and/or RBM experience.
  • This is what awaits YOU at J&J:

  • An opportunity to be part of a global market leader.
  • A dynamic and inspiring working environment.
  • Many opportunities to work on challenging projects and assignments.
  • Possibilities for further personal as well as professional development.
  • Many employee benefits.
  • Are you ready to impact the world?

    Johnson & Johnson offers an unusual experience to professionals looking for an opportunity to work with hardworking people who share your real passion for caring in an environment that empowers you to drive your own career.

    Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, or national origin and will not be discriminated against on the basis of disability.


    Información extra

    Status
    Inactiva
    Estudios requeridos
    Otros
    Localización
    madrid
    Horas a la semana
    8 - 40
    Tipo de contrato
    Tiempo completo
    Tipo de trabajo
    Marketing / Publicidad
    Carnet de conducir
    No
    Vehículo
    No
    Carta de motivación
    No
    Idiomas
    Español

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