Clinical Study Coordinator (Optometry) - Fort Worth TX

Overview

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

Responsibilities

• Maintain test and control article inventory throughout the study, and perform test and control article reconciliation at study completion.
• Manage the investigator file (ISF) and other regulatory documents throughout the study by obtaining essential documentation and complying to regulatory and sponsor requirements
• Participate in the SIM, site activation visits (SAV) and interim monitoring visits .
• Confirm all documents are available prior to study initiation meeting (SIM) and are complete at the study close-out
• Perform study procedures such as visual acuity,  topography, autorefractor commensurate with level of experience/training and as delegated by the PI and documented on the Site Delegation Log.
• Review and develop familiarity with protocol, study timelines, inclusion and exclusion criteria.
• Facilitate monitoring visits.
• Back-up for Clinical Research Scheduling Coordinator.
• Assure timely completion of Case Report Forms (CRFs) and responds to queries in a timely manner.
• Work with the PI to manage day to day activities of the study including subject scheduling, problem solving, communication and protocol management.
• Retain all study records in accordance with sponsor requirements.
• Work with PI to develop and implement recruitment strategies in accordance with IRB/IEC requirements.

Qualifications

• Bachelors degree or equivilant experience
• Clinical Research and/or understanding clinical trials
• Strong communication and collaboration skills

Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.