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Collaborating with CROs November 2012

Nov 9, 2012
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Course Description 

Outsourcing to Contract Research Organizations (CROs) to complete studies has become a foundation for pharmaceutical and device companies. With the lengthy drug development and approval process, it is nearly impossible to have complete study teams kept as full-time employees as the workload continually ebbs and flows. One of the challenges of outsourcing is selecting the right partner and then maintaining a team atmosphere where everyone takes ownership of the study. Key considerations when collaborating successfully with a CRO are selecting the right partner by knowing what questions to ask; establishing a foundation for the partnership with clear expectations, goals, and communication; and maintaining a sense of ownership in the work that has been outsourced. This web seminar will address the key criteria in selecting a partner, as well as review the necessary processes to foster positive relationships and allow for high quality performance of the CRO.

VideoPreview 

Learning Objectives 

  • Review key questions and selection criteria during the CRO evaluation and the request for proposal (RFP) review process
  • Explain the importance and various tools necessary for establishing clear expectations, communication, and objectives for the collaboration
  • Address techniques and oversight requirements to allow for a high performance alliance 

Who Should Attend 

  • Project Managers
  • Contract and Budget Management Personnel
  • Clinical Research Associate Managers
  • Clinical Research Associates
  • Directors in Clinical Operations
  • Site Managers 

Instructor 

Nikki Christison, B.S.

Click here for complete trainer biographies 

 

Hold this course at your company! For more information, contact Naila Ganatra at (215) 413-2471 

 

 

 

On-Demand GCP Refresher Training 

Too busy to attend a course? Our newly-released GCP eLearning course may be your solution!
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Barnett 'Hands-On' In-Person and Web Seminar Workshop Series
Barnett "Hands-On" Workshops are designed to provide intensive, hands-on training in a highly targeted clinical research topic area in a very interactive and engaging learning environment. To view more details and available courses, click here.


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Use of Notes to File in Clinical Trial Essential Documentation 

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PublicationsPUBLICATIONS

2012 GCP Question & Answer Guide Print Edition 

2012 Good Clinical Practice Question & Answer Guide Electronic Edition 

CFR/ICH GCP Reference Guide 2012 (Spiral Bound) 

CFR/ICH GCP Reference Guide 2012 (Perfect Bound) 

PAREXEL's Bio/Pharma R&D Statistical Sourcebook 2012/2013 (Hard Copy)