Principal Investigator
Spartanburg, SC

Currently seeking a talented and dedicated Principal Investigator for a great opportunity in the Spartanburg, SC area. 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.
State
SC
City
Spartanburg
Date Posted
3/24/2022
Job Type
Permanent