Study Participant Recruiter

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.

• Do you have a strong passion for assisting in the execution of all aspects of clinical trials? To fulfill your passion, we have an opportunity for you to join our growing team rated by Forbes as one of America's best employers for three years in a row!

ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build an outstanding career.

The Recruiter is responsible for recruitment activities for clinical trials and reporting recruitment status to ICON Develop Solutions - San Antonio (IDS - SAT). They are responsible for updating and maintaining the recruitment database, phone screening potential research subjects, and arranging appointments for potential research subjects. You will be responsible for performing the task(s) as per clinical trial, ICON Early Phase Services protocol SOPs, FDA, ICH, GCP and utilizing accurate source documentation techniques. Please note this position is on an as-needed basis.

What you will need:

• Minimum of a high school diploma or equivalent. Four-year degree preferred.
• Familiarity with ICH GCP and FDA Regulations. Science or medical knowledge is a plus
• 1 - 3 years of experience in the healthcare industry or clinical research preferred.
• A standout colleague with excellent social skills and strong interpersonal skills.
• Self-starter with the ability to work on their own initiative under tight timelines.
• Positive attitude with an excellent work ethic and attention to detail.

Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON 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.