Senior CRC

Recruiting now for a Senior Clinical Research Coordinator (CRC) at ICON, for Charleston location. This permanent opportunity, reports directly to the Clinical Operations Manager, with the primary aim; to coordinator multiple studies according to protocol, perform collection of clinical data points and to provide a seamless, customer service to the patients attending site.

In our mission as an Integrated Site Network, the role of our Coordinators are paramount. As a Senior CRC, you will be responsible, day to day for the following tasks:

• Performs study start-up duties including the production of a recruitment tool, and progress notes, as well as phone screening patients and identifying participants for trials on site
• Proactively develops and executes recruitment plans that meet and exceed enrollment goals
• Completes training on Clinical Trial Management System and maintains proper skills to update database, complete participant reimbursement, capture referral source of participants, and create calls lists to promote recruitment.
• Attends investigator meetings
• Performs technical requirements of the study protocol, i.e., lab work (phlebotomy and processing), blood pressure, electrocardiograms, Holtor monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or specified by a protocol
• Documents laboratory data and adverse reactions, presents this information to an investigator in a timely manner, and immediately notifies investigators, the Institutional Review Board and sponsor of any serious adverse events
• Builds and maintains strong relationships with Investigators and provides ongoing communication about trial status and participants