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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 organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization 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.

• 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.
• * Ability to work on study teams that are often virtual, multi-cultural , and multi-disciplinary
• *Serves as the primary contact for sites and investigators participating in studies
• *Acts as a resource for internal study teams and other ICON departments
• *Maintains, reviews, and ensures adequacy of information and data contained in site management reports, tracking systems (CTMS or others) and other site management documents
• *Conducts and completes remote site management activities, with support as needed, according to applicable SOPs and the Site Management Plan
• *Participates in QA audits as needed
• *Regularly attends and contributes to project specific and departmental meetings
• *Ability and willingness to travel as needed (drive and fly) - approximately 25% of the time
• *Reviews drug storage and drug accountab ility procedures (as applicable) , in accordance with applicable SOPs
• *Maintains and archives study documentation and correspondence , as needed
• *Assists with site contracting process, as needed
• *Assists with timely preparation and submission of regulatory documents for IRB/IEC submissions according to local requirements, with support, as needed
• *With support, demonstrates the ability to manage site assignments and workload
• *Maintains Sponsor and patient confidentiality
• *Actively participates in regular meetings with Project Managers or delegate, and/or RS Lead
• *Assists in development of site and patient enrolment strategies with project team; works to motivate sites to meet enrolment timelines
• *Developing knowledge of and compliance with local regulatory requirements
• *Compliant and current with departmental and corporate policies and procedures

COMMUNICATION
BUSINESS DEVELOPMENT
TEAMWORK
PERSONAL/PROFESSIONAL DEVELOPMENT
LEADERSHIP
MANAGERIAL/ ADMINISTRATIVE
ADAPT ABILITY
PROBLEM SOLVING
WORK QUALITY

- Degree in Health Science + Master degree in Clinical Trials

- Office based (Madrid or Barcelona)

- Fluent English

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.