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CRA II

ICON Strategic Solutions

Castellón de la Plana

Presencial

EUR 30.000 - 50.000

Jornada completa

Ayer

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Descripción de la vacante

A leading global clinical research organization is looking for a CRA II to monitor clinical trial sites effectively. This role requires experience in oncology clinical trials, proficiency in medical terminology, and the ability to ensure compliance with ICH/GCP guidelines. As a CRA II, you'll maintain strong relationships with study sites, ensuring the integrity and accuracy of clinical trial data while receiving competitive benefits that support your career and personal well-being.

Servicios

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible country-specific optional benefits

Formación

Experienced in Oncology clinical trials monitoring (2 years).
Working knowledge of Local Regulations and ICH/GCP Guidelines.
Strong technical skills with CTMS, eCRF, eTMF.

Responsabilidades

Monitor clinical trial sites and ensure adherence to GCP/ICH practices.
Review 'source to CRF/eCRF', ensuring patient safety and data integrity.
Collaborate with the team for project updates and timelines.

Conocimientos

Oncology clinical trials monitoring

Medical terminology

Record-keeping skills

Adaptability

Attention to detail

Educación

Scientific background

Herramientas

CTMS

eCRF

eTMF

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As a CRA II you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What You Will Be Doing

You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas. Assist other CRAs with co-monitoring activities both remote and on-site.
You will utilise your customer service mindset with your sites focusing on delivering value, building loyalty and trust to create a positive impact and strong relationship with investigators and study coordinators where respect, knowledge and commitment to ICH / GCP guidelines are key to successful trial conduct.
As the CRA you are the main sponsor representative, providing key project updates. You will collaborate with the team, developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely.
You will be first to review "source to CRF / eCRF," ensuring patient safety and data integrity aspect of the study.
As the first point of contact for study sites, escalating any concerns / issues to other departments including Safety, Investigational Medicinal Product, Local Study Managers and management team as appropriate.
Additionally, you will oversee the sites' adherence to GCP / ICH practices, ensuring quality of study conduct.

You Are

Experienced in Oncology clinical trials monitoring (2 years)
Scientific background
Proficiency with medical terminology
Working knowledge of Local Regulations
A demonstrated working knowledge of 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, eTMF

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.

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

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON : 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.

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. Seniority level

Seniority level Mid-Senior level

Employment type

Employment type Full-time

Job function

Job function Research, Analyst, and Information Technology
Industries Pharmaceutical Manufacturing

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