Covance

  • Sr Site Contract Specialist

    Job Location(s) BR
    Job Number
    2018-21574
    Job Category
    Clinical Operations
    Position Type
    Full-Time
  • Job Overview

    Senior Site Contract Specialist- Excellent position for experienced legal and financial professionals. Pharma or Research industry experience preferred - SAO PAULO, BRAZIL


    Come work as a Sr. Site Contract Specialist 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 Sr. Contract Specialist, experience in clinical research including working knowledge of ICH, FDA, IRB/IEC regulations required. This position requires that qualified candidates speak English fluently. We offer a competitive salary with benefits.

     

    Overview: Oversees administration and negotiation processes for complex site contracts that support projects within Clinical operations. Ensures site contact documentation is in compliance with sponsor and company requirements.

     

    Responsibilities/Duties:

     

    • Negotiates and prepares contracts, budgets and related documents for participation in industry-sponsored clinical trials.
    • Reviews contracts for completeness and accordance and ensure that corrections are correctly made and documented.
    • Assist Contract Managers with the active project management.
    • Generates amendment documents, as necessary.
    • Create and maintain document status, report and updates on a regular basis
    • Collaborate with internal and external legal, finance and project management departments

    Education/Qualifications

    Doctorate/University/College Degree

    Experience

    • 5 years of work experience in clinical research, including a strong working knowledge of ICH , FDA, IRB/IEC regulations
    • Excellent level of proficiency in English

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