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    Regional Study Coordinator - Indianapolis, United States - Labcorp

    Labcorp
    Labcorp Indianapolis, United States

    3 weeks ago

    Labcorp background
    Description

    The Regional Study Coordinator (RSC) is responsible for the successful delivery of all operations of a clinical study in their specific area of the world.

    The RSC acts as the appointed Liaison between Global Project Management, Client Representatives and other departments involved in the clinical study to ensure the successful management of regional study responsibilities.

    The Regional Study Coordinator may communication with the Client when a task is being delegated by the Global Study Manager.

    Regular communication is essential with the appointed Global Study Manager who is accountable for the entire protocol.

    This position must be in compliance with the Central Labs Global Project Management strategy and deliver outstanding customer satisfaction and performance.

    This position is remote and can be located anywhere in the US.


    Essential Job Duties:

    • Act as regional liaison between Global Study Manager and various CCLS departments involved in the study
    • Act as regional liaison between assigned Client representatives (eg. CRA, Site Monitors) and the corresponding local CCLS platform; occasionally, the Regional Study Coordinator can represent Global Study Manager in interactions with the main client contact
    • Close collaboration with the Global Study Manager for all study related aspects that are pertaining to the corresponding local platform and through all study stages, from set-up to closure
    • Review the study Statement of Work to ensure local feasibility and make appropriate recommendations to the Study Design Lead
    • Ensure a detailed knowledge of the SOW specifications and very good understanding of how the SOW specifications impact every operational aspect of the clinical trial
    • Manage day-to-day local study related activities, especially logistics, monitoring and study supplies, keeping the Global Study Manager informed of any study development
    • Monitor, track and provide resolution to all local study issues, keeping the Global Study Manager in the communication loop


    The Regional Study Coordinator is expected to interact internally on a regular basis and occasionally with external clients throughout all job duties mentioned above.


    Experience:


    • Must be fluent in both English and Mandarin languages
    • Bachelor's degree preferred but not required
    • At least two years of applicable experience
    • Demonstrated ability to plan and prioritize tasks and workload in a fast paced environment
    • Exceptional communication and organizational skills
    • Excellent attention to detail and teamwork orientation
    • Demonstrated ability to facilitate meetings and work with clients

    Application Window: Closes at the end of the day on May 31, 2024


    Work Location: US remote


    Pay Range: 60-75K per annum


    Benefits: All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Commissions, and Company bonus where applicable. For more detailed information, please click here )
    .

    Labcorp is proud to be an
    Equal Opportunity Employer:


    As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.

    We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.

    We encourage all to apply.

    For more information about how we collect and store your personal data, please see our Privacy Statement ) .
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