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    Clinical Medical Manager Team Lead (Manager)

    Novo Nordisk
    5+ years
    Not Disclosed
    Seoul
    10 Nov. 11, 2024
    Job Description
    Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Job Title: Clinical Medical Manager Team Lead/Manager

    Location: Novo Nordisk, South Korea
    Department: Medical Affairs Korea

    Are you a seasoned medical professional with expertise in clinical trials and therapeutic areas like Cardiovascular Disease, Chronic Kidney Disease, Liver Disease, Inflammation, Alzheimer’s Disease, and emerging therapy areas?

    If you are passionate about driving clinical trials, providing medical expertise, and leading a team to bring innovative treatments to life, this is the opportunity for you! Join us as a Clinical Medical Manager Team Lead/Manager at Novo Nordisk Korea, where you will have a significant role in shaping the future of healthcare and advancing clinical research.

    About the Department:

    The Medical Affairs Korea department at Novo Nordisk is a collaborative and dynamic team focused on advancing patient care through clinical research and innovation. We work closely with key opinion leaders (KOLs), investigators, research centers, and patient advocacy groups to drive clinical trials and improve healthcare outcomes. With opportunities for growth and professional development, this department is at the forefront of the company’s clinical efforts in South Korea and beyond.

    The Position:

    As the Clinical Medical Manager Team Lead/Manager, you will lead a team of Clinical Medical Managers (CMMs), providing guidance, support, and leadership across multiple therapeutic areas. Your role will include overseeing clinical trial execution, offering medical and scientific expertise, and ensuring alignment with global and regional strategies.

    Key Responsibilities:

    • Team Leadership: Manage the daily activities of the CMMs, guiding them on operations and priorities while ensuring they have the necessary capabilities to perform their duties effectively.
    • KOL and Investigator Engagement: Identify and map KOLs, investigators, and research centers in relevant therapeutic areas, developing engagement plans and fostering collaboration with external experts and professional associations.
    • Clinical Trial Support: Work closely with clinical operations teams to contribute to site selection, trial feasibility, and protocol development. Provide operational input and medical insights to optimize clinical trial execution.
    • Scientific Guidance: Engage with clinical experts to gather insights, ensuring proper training for site staff on the scientific background of trials. Lead scientific discussions and provide timely responses to internal and external stakeholders.
    • Investigator-Sponsored Studies: Support the Investigator Sponsored Studies (ISS) process and follow-up, ensuring smooth collaboration with the Medical Affairs team.
    • Training and Development: Provide medical training for internal teams, including CMMs and clinical staff, ensuring alignment with best practices and regulatory standards.

    Qualifications:

    To be considered for this role, you should meet the following criteria:

    • Education: MD, Ph.D., PharmD, or Pharmacist with a strong clinical and research background.
    • Experience: 8+ years of experience in the pharmaceutical industry or clinical research, with significant exposure to therapeutic areas like Cardiovascular Disease, Chronic Kidney Disease, Liver Disease, Alzheimer’s Disease, and more.
    • Clinical Experience: Experience as a clinical trial investigator or sub-investigator in Medical Affairs is preferred. Previous people management experience is essential.
    • Scientific Communication: Strong scientific communication skills, with the ability to engage effectively with both internal teams and external stakeholders, including KOLs and healthcare professionals.
    • Leadership: Proven ability to lead and mentor teams, driving collaboration and operational excellence across diverse functions.

    Working at Novo Nordisk:

    At Novo Nordisk, we don’t wait for change – we drive it. With a strong commitment to innovation, we empower our employees to challenge the status quo and push the boundaries of medical science. As a part of our team, you will have the opportunity to make a lasting impact on healthcare, both in South Korea and globally.

    Contact:

    For further information, please upload your CV via the Apply button on our online career page.

    Deadline:

    Applications will be reviewed on an ongoing basis. We encourage you to apply as soon as possible.

    Equal Opportunity Employer:

    At Novo Nordisk, we are committed to creating a diverse and inclusive workplace. We believe that a variety of perspectives and backgrounds contributes to the innovative solutions we provide to our patients.

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