Clinical Research Associate

CHEManager International; Paris; Hybride; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A leading clinical research organization is seeking an experienced Senior Clinical Research Associate to join their team in Paris/Ile-de-France. In this hybrid role, you will manage investigator sites and ensure compliance throughout clinical trials, particularly in Oncology. Candidates should have at least 24 months of independent monitoring experience and strong organizational skills. The position offers competitive salary and attractive benefits aimed at promoting work-life balance and well-being.

Prestations

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Qualifications

• Stable experience as a CRA in the pharmaceutical industry or a CRO.
• Experience in Oncology (Radioconjugate/Radiotherapy) therapeutic areas.
• Strong communication with the ability to multitask and work effectively under pressure.

Responsabilités

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

Connaissances

Experience as a CRA

Oncology experience

Excellent organization skills

Experience in Risk-Based Monitoring

Strong IT skills

Strong communication skills

Ability to multitask under pressure

Fluency in French

Professional proficiency in English

Description du poste

Senior Clinical Research Associate - France - Hybrid

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.

We are looking for motivated CRA II or Senior CRA based in the Paris/Ile‑de‑France area to join our sponsor dedicated CRA team!

You will demonstrate, minimum 24 months independent external monitoring of commercial studies in Oncology (Radio Conjugate/Radiotherapy).

Other therapeutic areas are also of interest, especially if gained on phase II‑III commercial trials.

The format will be 1‑3 days/week at the client office (day on site = office day).

As a CRA II or Senior CRA, you will be dedicated to one of our global pharmaceutical clients, with whom ICON shares a culture of innovation, flexibility and a common vision of bringing life‑improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in this exclusive program.

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 of drug safety issues.
• Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines.

We believe our Clinical Operations team is second to none. You will receive the support you need to develop personally and professionally and work in an environment where you matter. Our team pushes forward together. United in solving problems, developing close site relationships and reaching the end goal. Operating as a key part of a global study team, the CRA plays a fundamental role in our clients' drug development processes.

You Will Need

• A stable experience as a CRA, this within the pharmaceutical industry or a CRO
• Experience in Oncology (Radioconjugate/Radiotherapy) therapeutic areas
• Excellent organization skills
• Experience in RBM/RBQM (Risk‑Based Monitoring and Risk‑Based Quality Management)
• 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.

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 maximize 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 site to read more about the benefits ICON offers.

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.