Data Coordinator

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

With our patients at the center 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.

Data Coordinator:This position is responsible for timely completion of paper based or electronic case report forms, completing or facilitating the completion of all sponsor produced queries, performing quality control checks of case report forms prior to sponsor review and is the primary liaison for the Clinical Research Associate (CRA) during monitoring visits.

Responsibilities:

• Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance.• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.• Travel: Travel to other sites within the network may be required to support increases in workload and, or studies/projects as needed.• Represents data management at all internal and external meetings and providing data management updates as required.• Performs additional quality control checks prior to case report form completion.• Oversee CRA monitoring visit and complete or facilitate the completion of queries generated from visit.• Complete closure forms and packaging of source documents and case report forms at the end of assigned study.• Review and perform quality checks on subjects research chart for completion of case report forms.• Participate in internal and external audits as required.• Follow any reasonable directive from the Medical Director, PI and Clinical Data Services Supervisor.• To undertake other reasonable related duties as may be assigned from time to time.

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 through the form below.

e let us know through the form below.