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    Lead Clinical Research Associate - Lisbon, Portugal - Novo Nordisk

    Novo Nordisk
    Novo Nordisk Lisbon, Portugal

    há 4 semanas

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    Descrição
    The position

    Accountable for the independent country management clinical trial, for all its stages, to a high quality in accordance with the Company's policies and procedures, compliance with the clinical study protocol and local and global regulations and guidelines whilst maintaining the standards of the Novo Nordisk Way.

    Ensures the achievement of country study objectives in terms of timeliness, recruitment, performance, productivity and quality.


    Your main responsibilities will be:

    Act as the secondary point of contact between site staff and Novo Nordisk - act as ambassador for the company and contributes to making Novo Nordisk the preferred partner.

    Contribute to or drive Scientific Recruitment and Retention (SRR) planning and execution, in collaboration with CDC Trial Manager (TM) and site CRA as applicable and as agreed with Line Manager (LM).

    Overall country trial management, from site selection through close out. You will further be responsible for driving continuous improvement in projects.

    Contribute to local trial management activities, such as documents preparation and QC for submission to Health Authority (HA) and/ or Competent Ethics Committee (CEC), local trial budget alignment with CDC-TM or site contracts, as agreed with the LM.

    Co-monitor, train and coach less experienced members of the local team as agreed with LM and act as their back-up.

    This position will be preferably based in Lisbon, however the incumbent will be required to travel nationally as well as internationally and will report directly to the Clinical Head in Portugal.

    This is a permanent position.

    Qualifications To be effective in this role you need to have:
    University degree preferably within the Life Sciences or equivalent (biology, pharmacy, nursing etc). Minimum 4 years previous work experience as a Clinical Research Associate in the pharmaceutical industry or CROs. Preference for some degree of previous local trial management experience.

    Adequate English and Portuguese verbal and written skills Experience in cross-functional collaboration and teamwork Proficient analytical skills, result-oriented and problem-solving capability assuring quality mindset Pro-active and self-motivated Patient-centric mindset About the department In the Clinical Medical and Regulatory (CMR) department we drive change to defeat serious chronic diseases.

    In Clinical, we are committed to deliver clinical results of an exceptionally high standard, thereby contributing to the development of innovative medicines.

    Our exciting pipeline translates into a several-fold increase in R&D investment in Portugal, when comparing with .

    In Medical Affairs, we drive business with science and we partner for better care engaging with KOLs and HCPs who work daily with people living with chronic conditions.

    Finally, in Regulatory we ensure our license to operate and the supply of high-quality medications to people who need it the most.

    Working at Novo Nordisk Novo Nordisk is its people.

    We know that life is anything but linear and balancing what is important at different stages of our career is never easy.

    That's why we make room for diverse life situations, always putting people first.

    We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them.

    Working at Novo Nordisk is working toward something bigger than ourselves, and it's a collective effort. Novo Nordisk relies on the joint potential and collaboration of its employees. Together, we go further. Together, we're life changing.
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