Clinical Research Associate II

ICON Strategic Solutions; À distance; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading clinical research organization seeks a motivated Clinical Research Associate II based in France, offering a remote work model. This role requires at least 24 months of experience in independent external monitoring of commercial studies. You will manage investigator sites throughout the study lifecycle while ensuring compliance with clinical guidelines. Strong organizational and communication skills, alongside fluency in both French and English, are essential for success in this position. Additional benefits include a competitive salary and various health insurance offerings.

Prestations

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifications

• Minimum 24 months' experience as a CRA in the pharmaceutical industry or a CRO.
• Demonstrated independent external monitoring of commercial studies.
• Ability to multitask and work effectively under pressure.

Responsabilités

• Full ownership of investigator sites for assigned studies.
• Planning and conducting various site visits according to the clinical monitoring plan.
• Developing effective relationships with investigator site staff.

Connaissances

Excellent organization skills

Ability to work in a dynamic environment

Strong IT skills

Strong communication

Fluency in French

Professional proficiency in English

Description du poste

Clinical Research Associate II - France - Remote

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

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

We are looking for motivated Clinical Research Associate II or even Senior Clinical Research Associate based in France to join our dedicated CRA team! You will demonstrate, ideally at least 24 months independent external monitoring of commercial studies, especially if gained on phase II, III commercial trials.

Responsibilities

• Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close‑out.
• Planning and conducting various site visits (feasibility, site selection, interim and close‑out) in accordance with the clinical monitoring plan.
• Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
• Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following up on drug safety issues.
• Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines.

Qualifications

• Minimum 24 months' experience as a CRA, this within the pharmaceutical industry or a CRO
• Excellent organization skills
• Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business
• Strong IT skills
• Strong communication with the ability to multitask and work effectively under pressure
• Fluency in French and professional proficiency in English

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 maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.

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.

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.