• Clinical Trial Coordinator

    Job Location(s) GT
    Job Number
    Job Category
    Clinical Operations
    Position Type
    Hidden (2052)
  • Job Overview

    Clinical Trial Coordinator – Excellent opportunity for new research professionals looking to develop their careers in clinical research.

    Come work as a Clinical Trial Coordinator at the top Clinical Research Organization. We offer great benefits with opportunities to grow and learn alongside accomplished professionals.


    The Company - COVANCE


    As one of the world's largest and most comprehensive drug development services companies, Covance has helped pharmaceutical and biotech companies develop one-third of the all prescription drugs in the marketplace today.


    The Position


    We are looking for a full time Clinical Trial Coordinator, basic understanding of biology and biological processes is needed. Qualified applicants will have good organization/time management skills, good communication skills, fluent in English, general computer literacy.




    • Act as contact for project team and study sites.
    • Perform CRF review, query generation and resolution against established data review guidelines, under direct supervision on Covance or client data management systems, as assigned by management.
    • Assist with generation and reconciliation of queries to investigative sites/clients to resolve problem data.
    • Assist with the management of study supplies and organize shipments.
    • Create, update, track, and maintain study-specific trial management files, tools, and systems.
    • Assist the local project team members with other administrative activities as required (e.g. payments to investigators, correspondence with clients, preparation of status reports, and organization of investigators’ meetings).
    • Co-ordinate meetings with clients, investigators, and project team, including taking minutes.
    • Ensure compliance with Covance S.O.P.s, FDA, ICH, and GCP regulations for clinical conduct in all aspects of daily work.
    • Provide input in writing Monitoring Conventions as assigned.
    • Assist in submissions and notifications to Ethics Committees and Regulatory Authorities.

    General On-Site Monitoring Responsibilities:

    • Assist Senior CRAs, CRA-2 and CRA-1 with on-site tasks as required and according to training goals (e.g. review of Case Report Forms and Study File Notebook, drug accountability).
    • Initiate, monitor and close out clinical investigative sites under direct supervision from Clinical Research Associates 1 and 2, Sr. Clinical Research Associates, Project Managers or Project Directors.
    • Perform other duties as assigned by management.


    University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
    In lieu of the above requirement, candidates with one (1) or more years of relevant clinical research experience in pharmaceutical or CRO industries will be considered.


    One or more years of experience in a related field (i.e medical, clinical, pharmaceutical, laboratory, research, data analysis, data management, technical writing).


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