Training

Bright offers Training and Education programs to suit your organization's individual needs. Whether you require on-site training or large-scale seminars, we can prepare your staff for all stages of device and drug trial management, for the successful transaction from inception to research to FDA submission and eventual approval.

Our clinical trainers each have a minimum six years' experience in the clinical trials industry, and have worked in all areas of the field, including central roles at large and small pharmaceutical companies, biotechs, investigative sites, and within the FDA. They have worked with teams of all sizes, preparing them for the rigors of a clinical trial where accurate data capture and documentation are of the utmost importance.

We can devise a specialized course of training within the specific areas of your current needs, as well as universally valuable training courses such as:

• Clinical Research Associate Training
• Site Staff Training
• Patient Recruitment and Retention Workshops
• Advertising for Clinical Trials Training
• Working with IRBs
• Site Coordinator Workshops
• Phase I Trial Preparation and Organization
• GCP

• Regulatory Support
• Medical Writing
• Program Management
• Project Management
• Quality Management
• Safety
• Training
• Patient Recruitment
• Patient Retention
• Biostatistical Services
• Data Management
• Clinical Monitoring