Facilitate and coordinate the daily clinical trial activities
Actively recruit candidates for Women's Health Clinical Trials
Collaborate with the Principal Investigator, UWCR oversight team, sponsor, and host site to conduct all aspects of the clinical trials according to the protocol, FDA Regulations, ICH/GCP Guidelines, IRB policies and other governing authorities
Perform phlebotomy as required
Process, package and ship specimens, maintaining appropriate documentation
Dispense, retrieve, and reconcile investigational product
Document chain of custody for investigational product on appropriate logs
Promote teamwork, passion for clinical research, and standard of excellence throughout care center
3+ Years conducting Industry Clinical Trial
Experience in Women's Health is desired, but not required
Drive to succeed and commitment to standard of excellence required
Unified Women’s Clinical Research (UWCR) is a premier research organization that provides patients the opportunity to receive advanced medical care through participation in a variety of clinical trials. UWCR currently has research sites in North Carolina, Georgia and Florida with plans for expansion into Texas and Washington.
Our alliance with the largest and fastest growing group of Ob/Gyn pra...ctices across the nation enables UWCR to specialize in women’s health research including Gynecology, Uro-Gynecology, Obstetrics and Primary Care. This unique alliance provides our participants with comprehensive, collaborative care and our sponsors with unequivocal proficiency in trial execution.
Our investigators have accumulated over 20 years of experience working with over 50 sponsors conducting over 200 phase I-IV (first in human through post market) clinical trials on:
Investigational medications (intramuscular, intranasal, intrauterine, intravaginal, intravenous, subcutaneous, systemic, topical, transdermal)
We have also successfully completed numerous pharmacokinetic and observational studies.