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    Clinical Research Data Specialist 1 - Los Angeles, United States - Cedars-Sinai

    Cedars-Sinai
    Cedars-Sinai Los Angeles, United States

    1 month ago

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    Cedars-Sinai background
    Description

    Grow your career at Cedars-Sinai

    The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and niche care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.

    Join our team and use your skills with an organization known nationally for excellence in research

    The Clinical Research Data Specialist I manages the data for assigned research studies. This will include, crafting forms for data collection, clinical data abstraction, processing data, maintaining record systems, and producing project reports for studies. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.

    JOB DUTIES AND RESPONSIBILITIES:
    Manages data for research studies.

    Designs forms for data collection.

    Performs clinical data collection/abstraction.

    Processes clinical data using a range of computer applications and database systems to support cleaning and management of subject or patient data.

    Produces project reports.

    Maintains the accuracy, integrity and security of sophisticated, large computerized records systems.

    Understands regulations, policies, protocols and procedures to control and maintain accurate records.

    Performs data searches and other related administrative tasks.

    Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.

    Maintains research practices using Good Clinical Practice (GCP) guidelines.

    Maintains strict patient confidentiality according to HIPAA regulations and applicable law.

    Educational Requirements:

    Requires a bachelor's degree or equivalent in education, training and experience.

    Licenses: N/A

    Experience:

    :
    • Able to multitask in a diverse and demanding environment with frequently shifting priorities.

    • Proactive, extremely organized and detail oriented.

    • Strong record of interpersonal engagement.

    • Able to demonstrate the ability to balance both working independently and collaboratively.

    Physical Demands:


    • Able to perform moderate lifting.

    • Able to sit, stand and walk for prolonged periods of time.

    • Able to read papers and online documents.

    • Able to operate standard office equipment.

    • Able to exercise physical ability and perspective acuity to satisfactorily perform essential job functions.

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