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The Voice of the Site Coordinator
Industry Standard Research (ISR), Nov 2010, Pages: 130
Site Coordinators - more than any other person - have the power to drive the success of clinical studies. With on-the-ground responsibility for patient recruitment, informed consent, completing CRFs, managing queries, etc., understanding this group's perspective can make measurable differences to a pharma company's or CRO's development operations.
This report is based on primary market research data obtained by surveying 124 persons with responsibilities for site / study coordinator activities in the United States, Europe, Latin America and Asia. Respondents address in detail their ideas for:
- Enhancing patient recruitment efforts
- Developing closer relationships between sponsors and sites and CROs and sites
- Maintaining site engagement throughout the course of a clinical trial
- Improving feasibility estimates
and much more.
Sponsors and CROs can use this report to strengthen patient and investigator recruitment efforts, revamp feasibility processes and formulate a new and effective site relationship management approach.
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