Unblinded CRA II

ICON; Granada; Presencial; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

ICON, the world’s largest clinical research organization, seeks an Unblinded CRA to monitor clinical trial sites and ensure adherence to guidelines. Ideal candidates have a healthcare degree and relevant experience, particularly in Oncology. Join ICON for a competitive salary and benefits focused on well-being.

Servicios

Annual leave entitlements

Health insurance options for you and your family

Retirement planning options

24-hour employee assistance program

Flexible benefits like childcare vouchers and gym discounts

Formación

• 2-4 years relevant healthcare experience in pharma or clinical research.
• Strong experience in Oncology and site monitoring.
• Fluent in English, both written and oral.

Responsabilidades

• Monitor multiple Phase I, II, III, and IV clinical trial sites.
• Serve as the main sponsor representative providing project updates.
• Ensure adherence to GCP / ICH practices.

Conocimientos

Monitoring clinical trials

Customer service mindset

Attention to detail

Communication

Technical skills with CTMS

Educación

Bachelor’s Degree in a relevant field

Herramientas

CTMS

eCRF

eTMF systems

Descripción del empleo

As a Unblinded CRA, you will join the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence.

What you will be doing :

• Monitor multiple Phase I, II, III, and IV clinical trial sites, including pharmacy visits.
• Utilize your customer service mindset to focus on delivering value, building loyalty, and establishing trust with investigators and study coordinators, emphasizing respect, knowledge, and commitment to ICH / GCP guidelines for successful trial conduct.
• Serve as the main sponsor representative, providing key project updates, collaborating with the team, and developing commitment to study timelines and objectives through regular visits both in-person and remotely.
• Act as the first point of contact for study sites, escalating concerns / issues to relevant departments including Safety, Investigational Medicinal Product, Local Study Managers, and management as appropriate.
• Oversee sites' adherence to GCP / ICH practices, ensuring the quality of study conduct.

You are :

• Bachelor’s Degree (or equivalent) with 2-4 years of relevant healthcare experience in pharma or clinical research, including a minimum of 2 years monitoring and site management experience.
• Strong experience in Oncology and pharmacy visits.
• Experience in Phase I trials is a plus.
• Scientific background with proficiency in medical terminology.
• Working knowledge of local regulations and ICH / GCP guidelines.
• Excellent record-keeping skills and attention to detail.
• Experience conducting site selection, initiation, routine monitoring, and close-out visits both remotely and on-site.
• Fluent in English, both written and oral.
• Strong technical skills with CTMS, eCRF, and eTMF systems.

What ICON can offer you :

Our success depends on the quality of our people. We prioritize building a diverse culture that rewards high performance and nurtures talent.

In addition to a competitive salary, ICON offers various benefits focused on well-being and work-life balance, including :

• Annual leave entitlements
• Health insurance options for you and your family
• Retirement planning options to maximize savings
• Global Employee Assistance Programme through TELUS Health, offering 24-hour support from over 80,000 professionals
• Life assurance
• Flexible, country-specific benefits such as childcare vouchers, bike schemes, gym discounts, travel passes, health assessments, etc.

Learn more about working at ICON :

At ICON, inclusion and belonging are fundamental. We are committed to providing an inclusive, accessible environment free of discrimination and harassment. All qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. If you need reasonable accommodations during the application process or to perform job functions, please inform us via the provided link.

Interested but unsure if you meet all requirements? We encourage you to apply—your skills may be exactly what we’re looking for, whether for this role or others at ICON.

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