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    Principal Scientific Communications - Santa Clara, United States - Abbott Laboratories

    Abbott Laboratories
    Abbott Laboratories Santa Clara, United States

    1 week ago

    Abbott Laboratories background
    Description
    Abbott is a global healthcare leader that helps people live more fully at all stages of life.

    Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.

    Our 114,000 colleagues serve people in more than 160 countries.
    Principal Scientific Communications / Clinical Scientist

    Working at Abbott

    At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life.


    You'll also have access to:
    Career development with an international company where you can grow the career you dream of.

    Free medical coverage for employees* via the Health Investment Plan (HIP) PPO

    An excellent retirement savings plan with high employer contribution

    Tuition reimbursement, the

    Freedom 2 Save

    student debt program and

    FreeU

    education benefit - an affordable and convenient path to getting a bachelor's degree.


    A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.


    A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

    The Opportunity

    This position works out of our Santa Clara, CA., location, and can also be based in the Minneapolis/St Paul area, in the Structural Heart (SH) Division.


    Our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease.


    We have an exciting opportunity for the right candidate to join our rapidly growing clinical team within the SH division.

    The Scientific Communications/Clinical Scientist will be responsible for producing podium presentations, scientific publications, and clinical study reports for global regulatory submission using clinical data sets.

    The work will directly support evidence generation for transcatheter aortic valve implantation (TAVI) program. This position will work collaboratively with clinical scientists, biostatisticians, marketing, and other cross-functional leads.

    This position will also play a supporting role in interacting with clinical trial investigators to ensure the successful execution of clinical strategies to meet corporate podium and publication goals.

    What You'll Work On


    This position will work closely with cross-functional stakeholders in marketing, medical affairs, clinical affairs, biometrics, project management, data management, and other clinical groups.

    This position will also interact with physicians and regulatory authorities. Furthermore, this position will be required to execute the job responsibilities within the corporate policies and standard operating procedures.


    This position will:
    Responsible and accountable for execution of podium presentations, scientific publications, clinical study report writing for regulatory submission in collaboration with clinical program director and scientists

    Ensure cross-functional alignment of prioritization of clinical evidence dissemination

    Effectively communicate information through the planning and execution of meetings and presentations and present recommendations to all stakeholders

    Ensure internal stakeholders are up to date on all activities supporting podium presentations (conference acceptances, presentation status) and publications status as well as clinical study report review

    Drive internal and external collaborators to meet submission deadlines for conferences and journal submissions

    Drive activities to meet the deadlines for internal approvals of clinical study reports for regulatory submissions

    Oversee responses to journal reviewers and ensure they are handled in a timely manner

    Ensure all data presented is cohesive and in alignment with Abbott standards

    Support publication committee activities (planning and strategy) for key trials

    Plays a key role in KOL management through strategic engagement while maintaining a collaborative relationship

    Develops and maintains current, in-depth, relevant functional knowledge (such as scientific and technical aspects) of projects in support of the business on a global basis

    Will perform this job in a quality system environment.

    Prioritization across teams to ensure strategic goals/milestones within Clinical Affairs are met

    Works with stakeholders to define business questions, requirements, timelines, objectives, and success criteria to address the need

    Required Qualifications
    Bachelor's degree required; advanced degree preferred; degree in science, medicine, or a similar discipline is highly preferred.

    Minimum of 8+ years of related work experience in clinical trials/medical writing

    Cardiovascular and structural heart knowledge is a plus.


    • Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.
    Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:


    Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life.

    Abbott is an Equal Opportunity Employer, committed to employee diversity.
    Connect with us at

    , on Facebook at

    and on X @AbbottNews.


    The base pay for this position is $109,300.00 – $218, In specific locations, the pay range may vary from the range posted.

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