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Managing Vendor/CRO Oversight

Effectively Managing CROs/Vendors during Clinical Trials in GCP Compliance

7-8 May 2019
NBC Tower | Chicago, IL, United States of America


Why You Should Attend

Managing Vendor/CRO Oversight

Forming quality partnerships between pharma’s and CROs is essential to executing clinical trials in an efficient manner.  There must be a commitment from both the sponsor company and the CRO to form a partnership.  By implementing agreements on experience levels of study team staff, focusing on important KPIs, trusting the operational team staff to perform their responsibilities, creating short- and long-term milestones, and setting clear roles and responsibilities, the parties can improve their chance of achieving a successful partnership. 

 

Key Topics

  • CRO Industry Background and Regulatory Expectations
  • Vendor/CRO Selection - Assessing Compency of the Vendor/CRO
  • Managing the Vendor/CRO Project
  • Oversight Preparation, Planning, and Clarity of Roles and Responsibilites
  • On-gonig Oversight and Management
  • Previous Attendees Include

    Johnson & Johnson Inc.
    Pfizer Inc.
    Takeda Oncology
    Novartis Oncology
    Horizon Pharma
    American Heart Association
    Biogen
    Biomarin
    Cavion Inc.
    Clinical Trials of TexasGenentech
    Allergan
    Alnylam Pharmaceuticals
    Merck Sharp & Dohme - Columbia
    Horizon Pharma


    Why Choose marcus evans?

    marcus evans specialises in the research and development of strategic events for senior business executives. From our international network of 63 offices, marcus evans produces over 1000 event days a year on strategic issues in corporate finance, telecommunications, technology, health, transportation, capital markets, human resources and business improvement.

    Above all, marcus evans provides clients with business information and knowledge which enables them to sustain a valuable competitive advantage and makes a positive contribution to their success.






    Practical Insights From

    Scott Maurer
    Consultant
    Scott Maurer has held positions as an employee and consultant in the pharmaceutical, biotech, and device arena. Having worked for large and small companies as well as CRO's, he has contributed to high visibility projects leading to more than a dozen drub, device, and biotech approvals.

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    Event Contact

    For all enquiries regarding speaking, sponsoring and attending this conference contact:

    Emily Jones


    marcusevans, The NBC Tower
    455 N. Cityfront Plaza Dr.
    Chicago, IL 60611

    Telephone:
    312.540.3000 x6714
    Fax: 312.894.6304
    Email: emilyj@marcusevansch.com