Senior CRA

ICON Strategic Solutions; France; Sur place; EUR 45 000 - 65 000; Plein temps

Avantages offerts par ce poste

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible country-specific benefits

Résumé du poste

A global clinical research organization is seeking a Senior Clinical Research Associate to oversee clinical trial sites with a focus on Oncology. The ideal candidate will have a Bachelor's degree and a strong background in monitoring and site management, with the ability to communicate effectively in English and French. This full-time role offers a competitive salary and various benefits that focus on well-being and work-life balance.

Qualifications

• Minimum 4 years of relevant healthcare experience in pharma or clinical research.
• Minimum 3/4 years of monitoring and site management experience.
• Proficiency with medical terminology.

Responsabilités

• Monitor multiple Phase I, II, III & IV clinical trial sites.
• Collaborate with the team, developing commitment to study timelines.
• Ensure patient safety and data integrity of the study.

Connaissances

Therapeutic knowledge in Oncology

Customer service mindset

Excellent record-keeping skills

Strong technical skills with CTMS

Fluent in English

Fluent in French

Fluent in Spanish

Formation

Bachelor’s degree (or equivalent)

Outils

CTMS

eCRF

eTMF

Description du poste

Overview

Join to apply for the Senior CRA role at ICON Strategic Solutions.

As a Senior CRA / Clinical Site Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You’ll utilise your extensive therapeutic knowledge in Oncology to oversee uniquely-focused clinical studies. Working at the core of clinical research, you’ll be exposed to cutting-edge protocols and experience a dedicated partnership with your team like never before.

Responsibilities

• You will monitor multiple Phase I, II, III & IV clinical trial sites (Spain and France).
• 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.

Qualifications

• Bachelor’s Degree (or equivalent) with +4 years of relevant healthcare experience in the pharma or clinical research industry. Minimum 3/4 years of monitoring and site management experience.
• Therapeutic Area: Oncology
• Scientific background
• Proficiency with medical terminology
• Working knowledge of Local Regulations
• 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; French (mandatory); and local language (Spanish).
• 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.

Benefits Examples

• 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: careers iconplc com/benefits

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, colour, 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.

Reasonable accommodations: careers iconplc com/reasonable-accommodations

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.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Research, Analyst, and Information Technology
• Industries: Pharmaceutical Manufacturing

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