Job board of the American Society for Clinical Investigation
Velocity Clinical Research: Principal Investigator
Principal Investigator
Spokane WA, Spartanburg SC, Austin TX, Cleveland OH
Currently seeking a talented and dedicated Principal Investigator for a great opportunity. The ideal candidate will possess 1 year of current experience working in a clinical research organization and have 5+ years of experience working in a scientific or research or healthcare environment
About Our Client:
Velocity Clinical Research
Velocity controls the process of conducting clinical trials by managing dedicated research sites. The Velocity model delivers: Superior, accelerated enrollment and consistent, reliable results. They operate 29 wholly owned institutions, dedicated to research, across 13 states. They have completed 7,000+ trials. Velocity's mission is to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high-quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.
Responsibilities of the Principal Investigator
- Provide overall medical direction and medical review of protocols in conformance with the investigational plan and good clinical practice
- Provide medical and scientific feasibility of all new sponsor inquiries
- Ensure that the safety and well-being of all participants in the study at the trial site are protected
- Ensure data collected at the study site is credible and accurate
- Ensure the rights, integrity, and confidentiality of all participants in the trial at the site are protected
- Assist and provide guidance to clinical operations, research staff, and to sponsor client managers as required
Requirements of Principal Investigator
- 1+ years of current experience working in a clinical research organization
- 5+ years of experience working in a scientific or research or healthcare environment
- M.D. is required
- Must have industry research experience and industry-sponsored clinical trials
- Must have been responsible for the conduct of clinical research that conforms with standards for Good Clinical Practice
- Must have experience and training in the conduct of clinical research
- Understanding of regulatory requirements, principles of GCP, and biomedical research ethics.
Contact information:
Julian Rives
info@chapelhillsolutions.com
Applications: