Research Associate FT - San Antonio

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.

Research Associate:

• 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 (approximately 5%) domestic and/or international.
• Familiarize, understand and apply all SOPs applicable to job description.
• Ability to understand protocol requirements.
• *Participate in the early planning phase of clinical study by providing assistance to the Clinical Research Coordinator and Study Manager.
• *Assist in preparation of study source document charts, screening packets, maintain clinical study enrollment logs, study status logs, payment and tracking logs, assist in filing documents, assists in query resolution.
• *Assist in admit set up (prepare arm bands, room assignments, coordinate training with clinical staff and help to conduct trainings.
• *Attend and assist with Study Team meetings to include (pre-study, Site Initiation, mock runs and Clinical Start-up Meetings).
• *Assist with Clinical Start-up Meetings and training with Clinical Staff.
• *Assist with quality checks on source documents and all trail related material.
• *Assist whit phone contacts to subjects.

• *Assist with review of screening charts to assure all required results have been filed and verify that subject qualifies for enrollment
• *Coordinate study specific events with vendors as assigned.
• *Participate in sponsor and monitor visits ad required by the Clinical Research Coordinator or Study Manager.
• To undertake other reasonably related duties as may be assigned from time to time from the Clinical Research Coordinator, Study Manager, Manger of Study Management, Director of Clinical Operations or other Manager/Supervisors and Investigators.
• *Assist the Clinical Research Coordinator/Study Manager as necessary to assist in oversight when needed to ensure the proper execution of the clinical trial, to include but not limited to:
a. Ensuring the clinical trial activities are executed as outlined in the clinical trial protocol;
b. Ensuring proper documentation of all procedures;

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.