Covance

  • Senior Clinical Project Administrator

    Job Location(s) CN-Shanghai
    Job Number
    2018-20837
    Job Category
    Administration/Clerical
    Position Type
    Full-Time
  • Job Overview

    Are you a Clinical Project Administrator who wants to work with one of leading global CROs in the industry? Whether you’re ready to make a move or just interested in learning more, apply TODAY and let’s talk together!

     

    Covance China is committed to providing a clinical research career with purpose in a culture that values achievement. By joining our Clinical Trial Operations Team, you will work in a collaborative environment with the flexibility to pursue different clinical trials involving various compounds - giving you an excellent overview of best practices across the industry. Experience the global reach and therapeutic record of success from one of the few truly global drug development companies positioned to provide comprehensive clinical support from First-in-Human studies.

     

    Responsibilities/Duties:

    Responsibilities and duties include, but are not limited to the following:

    1. Responsible for study documents filing, tracking and archiving and ensure these activities performed in compliance with GCP/SOPs and local regulation.
    2. Responsible for study administrative supports in compliance with according company policy and local regulation
    3. Providing general administrative supports to CRAs and line manager
    4. Establish and maintain sound working relationships with external (supplies, agency) and internal customers (finance, IT) to provide required supports to clinical trials
    5. This role should understand company's compliance and SHE policy, and to manage the daily activity to align with these accordingly.

    Education/Qualifications

    • Minimum one year administrative experience or equivalent training
    • Good oral and written communication skills.

    Experience

    • Minimum of four (4) years administrative experience in n corporate environment or, minimum of four (4) years Clinical Project Administrator experience
    • Demonstrated aptitude for training
    • Good oral and written communication skills
    • Ability to set priorities and handle multiple tasks simultaneously
    • Good organizational nnd time management skills
    • Computer literacy (word processing and spreadsheet software)
    • Good typing skills
    • Good spelling and proofreading skills
    • Aptitude for handling and reviewing numerical data
    • Ability to operate standard office equipment (e.g., fax, copier)
    • Works efficiently nnd effectively in a mntrix environment
    • Fluent in local office language nnd in English, both written and verbal

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