Clinical Development Consultant

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.

In this role, you will be part of our Strategic Solutions Division and be directly partnering with one of our top pharmaceutical sponsors with the support of ICON right behind you.

The Clinical Development Consultant (CDC) is responsible for the management of clinical sites being considered and/or
participating in Lilly clinical trials; inclusive of site identification and qualification, the timely delivery of clinical trial
enrollment in accordance with scientific objectives, timely delivery of database locks, issues management at clinical trial
sites, and ensuring inspection readiness at all times for assigned therapeutic area(s) within a region/country that enables
global program delivery. This is achieved by the CDC’s accountability for comprehensive site management, leveraging of
information/tools to make/have informed decisions and discussions, and high quality interactions with global clinical trial
sites to drive to an unparalled customer experience. The CDC is also responsible for oversight of vendor monitoring
activities at clinical trial sites, including the identification, mitigation and escalation of significant findings and trends.
Additional local responsibilities may be required as needed/appropriate for the local geography.

• Bachelor’s degree or equivalent in a scientific or health-related field
• Minimum of 3 years experience in the pharmaceutical industry and/or clinical research and strong working knowledge of
Good Clinical Practice
• Therapeutic expertise and knowledge of the clinical research landscape; ability to acquire and maintain therapeutic
expertise to support portfolio needs
• Strong self-management and organizational skills; ability to manage workload, set personal priorities and adjust as needed
• Demonstrated strategic agility & broad business acumen
• Demonstrated leadership behaviours with ability to accept challenges, seek opportunities to remove barriers, influence
without authority, and lead in areas of uncertainity