Senior CRA

ICON; Cartagena; Presencial; EUR 35.000 - 55.000; Jornada completa

Descripción de la vacante

A leading clinical research organization seeks a Sr. Clinical Research Associate (CRA) to monitor clinical trial sites and collaborate with study teams. The role requires strong attention to detail, a scientific background, and proficiency in medical terminology. Candidates should have 4-6 years of experience in clinical trials and be well-versed in ICH/GCP guidelines. Competitive salary and benefits offered.

Servicios

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Formación

• 4-6 years of relevant clinical trials monitoring experience.
• Demonstrated working knowledge of ICH / GCP Guidelines.
• Experience conducting Site Selection, Initiation, Routine Monitoring, and Close Out Visits.

Responsabilidades

• Monitor multiple Phase I, II, III & IV clinical trial sites.
• Ensure adherence to GCP / ICH practices.
• Provide key project updates to sponsors and escalate issues.

Conocimientos

Attention to detail

Proficiency with medical terminology

Scientific background

Strong technical skills

Educación

Bachelor’s Degree or equivalent

Herramientas

CTMS

eCRF

eTMF

Descripción del empleo

As a Sr. CRA 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 :

• Bachelor’s Degree (or equivalent) with 4-6 years of relevant clinical trials monitoring experience.
• 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.

• 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.

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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 through the form below.

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.

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