Covance

  • Senior Manager Clinical Operations, Ukraine

    Job Location(s) UA
    Job Number
    2018-20971
    Job Category
    Clinical Operations
    Position Type
    Full-Time
  • Job Overview

    As a Senior Manager, Clinical Operations, you would be responsible for the supervision of of assigned direct reports within Clinical Operations, CoSource and/or Global Site Services as well as the Sponsor interaction.

     

    Key Responsiblities:

    • Responsible for detailed performance review and management of assigned direct reports including: Annual Performance Management and Development (PMD), Individual Development Plan (IDP), Line of Sight Goals and “Shoves & Tugs”
    • Responsible for appropriate management and resolution of performance issues
    • Develop and measure performance indicators for assigned staff
    • Identify individual training needs and assist with the coordination and conduct of training and development efforts, regionally
    • Coordinate, conduct, report and follow-up on Quality Control Visits (CQC)
    • Effectively communicate management strategies, policies and procedures in conjunction with leadership teams
    • Develop and maintain effective relationships with management team to manage assigned staff in a matrix environment
    • Maintain good working relationships with internal and external clients to ensure opportunity for acquiring additional new business

    Education / Qualifications

    • University/college degree – life sciences 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 this required educational background the following relevant work history may be considered:
    • Minimum of five (5) years supervisory experience in a health care or clinical research setting and
    • Minimum of nine (9) years relevant clinical research experience in a pharmaceutical company/CRO

    Experience

    • Relevant clinical research experience in a pharmaceutical company or CRO
    • Individual is proficient with on site monitoring activities (including pre-study, initiation, routine monitoring and closeout visits)
    • Minimum of seven (7) years relevant clinical research experience in a pharmaceutical company/CRO
    • Thorough knowledge of drug development process
    • Thorough knowledge of relevant SOPs, ICH, and GCP guidelines
    • Relevant supervisory experience
    • Minimum of 3 years as a Line Manager or Project Manager required
    • Demonstrated ability to lead by example and to encourage team members to seek solutions
    • Proven interpersonal skills
    • Demonstrated ability to successfully participate as a member of a project team
    • Demonstrated ability to successfully manage multiple competing priorities
    • Advanced planning and organizational skills
    • Advanced oral, written and presentation skills

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