Covance

  • Manager, Clinical Operations - Turkey

    Job Location(s) TR-Istanbul
    Job Number
    2018-21525
    Job Category
    Clinical Operations
    Position Type
    Full-Time
  • Job Overview

    Get ready to redefine what’s possible and discover your extraordinary potential at Covance. Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.

     

     

    Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career.



    We are currently looking for Manager, Clinical Operations. 
     
    Key responsibilities: 
     

    1. Management and conduct of on-site Monitoring Quality Control for FSP staff
    2. Responsible for dotted-line management
    3. Serves as primary point of contact for FSP leadership team
    4. Responsible for developing and maintaining close ties with Quality Assurance group Measure performance indicators for assigned staff
    5. Escalate potential individual training needs and assist in the conduct of training and development efforts, regionally
    6. Effectively communicate management strategies, policies and procedures in conjunction with leadership teams
    7. Maintain good working relationships with internal and external clients to ensure opportunity for acquiring additional new business

    May be responsible for the supervision of assigned direct reports, which would include: o Responsibility for detailed performance review and management of assigned direct reports including: Annual Performance Management and Development (PMD)

     

    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)

     

     

    Experience

     

    • Relevant clinical research experience in a pharmaceutical company or CRO
    • Proficiency with on-site monitoring activities (including pre-study, initiation, routine monitoring and closeout visits)
    • Substantial 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
    • Some experience as a Line Manager or Project Manager preferred
    • 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
    • Excellent planning and organizational skills
    • Excellent oral, written and presentation skills

     

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