SITE RECRUITMENT

SITE RECRUITMENT

Dobbs Consulting has extensive experience in executing feasibility studies and performing site recruitment.  We believe that robust feasibility and meticulous, detailed investigator recruitment are essential to a successful trial.

We have built relationships with key opinion leaders as well as small community centers within the U.S. and Canada across a host of therapeutic areas; this allows us to provide the most accurate feasibility data to our clients and to recommend research sites that are best suited for a study's individualized needs. 

Dobbs Consulting has the capability of providing global feasibility studies for oncology trials through our association with other well-respected CROs.
Evaluation and Planning
  • Feasibility/Site Recruitment
  • Establish staffing needs
  • Identify team members
  • Investigator Meeting Planning
  • Administrative set-up
  • Team/Site Contact List
  • Monitoring Visit Schedule
  • Budget Tracking
  • Regulatory Document Collection and Submission
  • Trip Report Review and Tracking
  • Conduct internal and client kick-off meetings
  • Develop Monitoring Plan, Study Manual, Pharmacy Manual, and Source Documents
  • Establish time lines and set milestones
  • Train project team
  • Select vendors (data management, IRBs, central labs, pharmacovigilance, etc.) 
Execution and Management
  • Provide on-time deliverables
  • Conduct team teleconferences as required
  • Identify and resolve issues
  • Disseminate information
  • Facilitate communications, newsletters, supply management and vendor management
  • Quality Assessment
  • Flag activities that may compromise timelines