OMNI Human Resource Management

  • Clinical Data Coordinator I

    Job ID
    Vince & Associates Clinical Research
    Job Location(s)
    US-KS-Overland Park
  • Overview

    Altasciences- Vince and Asso

    Do you want a fast-paced, exciting and innovative career in research? Vince and Associates Clinical Research is currently looking for a Clinical Data Coordinator I for their Overland Park, KS campus.


    Altasciences Clinical Research, encompassing Algorithme Pharma, Vince and Associates Clinical Research and Algorithme Pharma USA, is one of the largest early phase clinical research organizations (CROs) in North America. As a leading, full-service CRO, we have extensive expertise in the execution of a wide range of Phase I/II clinical studies, especially complex trials in healthy normal volunteers and patient populations.


    The Clinical Data Coordinator is responsible for entering clinical study data and associated information into databases as well as perform other administrative duties within a clinical research office setting. This position proofreads information for accuracy and as updates data as information changes.




    • Review and understand all on-going study protocol and direction
    • Coordinate and track all information, communications, documents, and timelines for assigned projects or clinical studies
    • Take the initiative to ensure all data is being entered consistently and accurately within the database and assigned study documents
    • Communication to the data entry team on database issues occurring in real time- escalating more severe or disruptive issues and to a Data Entry department manager
    • Enter data into various databases after verification of legibility, completeness, and accuracy of the clinical data
    • Assist in maintaining internal systems and tracking tools, including providing status and activity reports as required
    • Communicate effectively with internal and external clients



    • High school Diploma or GED and a College Degree
    • 1 to 2 years data entry experience in a clinical trial setting
    • Experience in electronic data capture in clinical trials databases


    • Intermediate proficiency in Microsoft Office (Excel and Word specifically)
    • Technical problem solving and critical thinking skills
    • Ability to understand and follow standard operating procedures and protocol
    • Ability to multitask in fast- paced work environment.
    • Strong attention to detail

    All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, and protected veteran status, or disability status.


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