RAISING THE BAR

 

SITE MANAGEMENT AND CLINICAL MONITORING

CurAccel’s Site Management and Clinical Monitoring services provide a hands-on tactic when collaborating and coordinating with investigative sites.  Our monitoring team are the eyes and ears of the client to be a dedicated resource, clarify the plan, link the objectives to the tasks, compare the actuals with the target, and prepare the site for an audit.  As a result, monitoring is performed at a high throughput.

CurAccel can operate as a functional service provider or on a standalone basis.  At a minimum, our Site Management and Clinical Monitoring service offerings are:

  • Confidential Disclosure Agreement

  • Site identification, feasibility, and selection

  • Clinical trial planning and design (including risk-mitigation analysis)

  • Patient recruitment

  • Clinical on-site monitoring

 

Our Clinical Trial Managers (CTMs) are assigned at the earl earliest stages of project feasibility to assist in scope management to define and align the needs of your project.  Our CTMs will:

  • Hold an average of 8 years of industry and task-related experience

  • Serve as the monitoring manager for consistency and continuity

  • Develop and encourage the monitoring team to be functional and cohesive

  • Maximize the effectiveness of the monitoring team

 

Our Clinical Research Associates (CRAs) are assigned at the earliest stages of project feasibility to assist in identifying potential investigators and investigative sites.  Our CRAs will:

  • Hold an average of 5 years of industry and task-related experience

  • Serve as the primary point to the clinical investigators and sites

  • Represent you at the clinical site

  • Utilize ‘Best Practices’ effectively and efficiently

Phone: 877 757 3393

Fax: 877-567-1047

CurAccel, LLC

6 Penns Trail  Suite 202 Newtown, PA 18940