The English-language job board for Spain
88,000+ live jobsPermanent contract
Per the ad.
Hybrid
Office and home days — the ad has the split.
Have the right to work in Spain
ICON plc doesn't mention sponsorship in the ad.
Work in English
English is required, per the ad.
Czech
The ad asks for Czech, or counts it in your favour.
Hungarian
The ad asks for Hungarian, or counts it in your favour.
Be near Czech Republic, Prague for hybrid days
No relocation package mentioned.
University degree
“Bachelor's degree in life sciences, healthcare, business, or a related field, or equivalent clinical research experience.” — per the ad.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
Fluency in English
Bachelor's degree in life sciences, healthcare, business, or a related field, or equivalent clinical research experience.
Relevant experience in site support, clinical administration, or similar roles within CRO, pharma, or healthcare.
Good understanding of clinical trial processes, GCP, and site documentation requirements.
Strong organizational and problem-solving skills, with the ability to manage multiple countries/sites and priorities.
Excellent communication and interpersonal skills, with a proactive, service-focused mindset.
Comfort working independently while collaborating effectively with cross-functional teams.
What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
Proficiency in Czech, Hungarian, or another European language will be a great advantage.
We are currently seeking a Site Specialist to join our diverse and dynamic team. As a Site Specialist at ICON, you will independently manage a range of site support activities, acting as a key operational contact for sites and contributing to efficient study start-up and maintenance.
Coordinating site-level document collection, review, and maintenance, ensuring accuracy and compliance for assigned sites or studies.
Acting as an operational liaison for site staff on documentation, systems, and process-related questions.
Maintaining up-to-date site status, metrics, and key milestones in clinical trial management tools.
Support both internal and external stakeholders with submission-related coordination activities.
Identify opportunities to improve workflows and contribute to process optimization initiatives.
Actively share insights and learnings with the broader team to encourage continuous development and alignment.
Site Specialist II
Job Advert Posting
Visit our careers site to
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 or submit a request here
or browse Junior·Hybrid·Clinical research
This role involves monitoring clinical trials and ensuring protocol compliance and data integrity. ICON offers career development, a collaborative environment, and various well-being benefits.
As a Study Start Up Associate II, you will lead clinical trial initiation and ensure regulatory compliance. The role offers competitive salary and various well-being benefits.
As a Senior Clinical Associate, you will oversee and support the execution of clinical trials. The role offers career development and a collaborative environment.
You will oversee regulatory affairs delivery, coach teams, and design clinical trials. The role offers competitive salary and various well-being benefits. This position is based in Mechelen, Belgium.
Clinical Trial Assistant to support clinical trial site management and monitoring activities. The role offers career development and a collaborative environment in Madrid.
Clinical Research Associates design and analyze clinical trials while interpreting complex medical data. The role offers career development and a collaborative environment.
Clinical Research Associate II will design and analyse clinical trials and monitor site activities. The role offers career development and a collaborative environment.
A Clinical Research Associate II will design and analyze clinical trials and monitor site activities. The role offers career development and a collaborative environment.
Senior Clinical Research Associate overseeing clinical trial activities to ensure protocol and regulatory compliance.
This role manages clinical trial start-up and site activation activities to meet client objectives. It offers career development, a collaborative environment, and various well-being benefits.
This role manages site payments and subject reimbursements for clinical studies. It offers career development and a collaborative environment. The position is remote-based.
This role supports clients seeking to license and implement Clinical Outcome Assessments in research. You will manage client requests, prepare proposals, and coordinate project activities.
€69k - €128k
Blue Card threshold🇬🇧€49k - €80k
Blue Card threshold🇬🇧€40k - €59k
🇬🇧€73k - €136k
🇬🇧€46k - €58k
Blue Card threshold🇬🇧 🇪🇸€30k - €33k
🇬🇧
