Recruiting now for a Clinical Research Coordinator Level 1 (CRC) at ICON, for Bristol location. This full time temporary opportunity, reports directly to the Clinical Operations Manager, with the primary aim;
to coordinate multiple studies according to the study protocol, perform collection of clinical data points and to provide a seamless, customer service to the patients attending site.
Our mission is to function as an Integrated Site Network, the role of our Coordinators are paramount to achieving our mission.
As a CRC Level 1, 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
Successful applicants will have the following :
Bachelor's life science degree, or relevant industry-field experience
1 years' work experience in clinical research or pharmaceutical environment would be desirable
High level of attention to detail
Personable, able to build rapport with patients with ease
Motivated about a career in clinical research
Excellent planner, organized approach to work
Following your application, we will contact you and one of our dedicated recruiters will be able to provide you with more details about this opportunity.
ICON is an equal opportunity employer - Minorities / Females / Disabled / Veterans and committed to providing a workplace free of any discrimination or harassment.