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