Senior Clinical Research Associate

Pharmaceutical Research Associates, Inc; France; Hybride; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading clinical research organization is seeking a Senior Clinical Research Associate to join their dedicated team in Paris. This role requires a minimum of 4-5 years experience in Oncology studies, monitoring commercial trials. Responsibilities include managing investigator sites, conducting site visits, and ensuring compliance with clinical guidelines. The organization offers competitive salary and a variety of benefits focused on well-being and work-life balance.

Prestations

Various annual leave entitlements

Health insurance offerings

Retirement planning offerings

Employee Assistance Programme

Flexible optional benefits

Qualifications

• Minimum 4-5 years experience with external monitoring of commercial studies in Oncology.
• Solid experience as a Senior CRA within a pharmaceutical company or CRO.
• Strong IT skills.

Responsabilités

• Full ownership of investigator sites from study initiation to close-out.
• Conduct feasibility, site selection, interim, and close-out visits.
• Monitor data integrity and compliance with clinical trial guidelines.

Connaissances

Oncology expertise

Experience in RBM/RBQM

Fluency in French

Professional proficiency in English

Strong organizational skills

Multitasking under pressure

Description du poste

Overview

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

Responsibilities

We are looking for motivated CRAs based in the Paris/Ile-de-France area to join our sponsor dedicated CRA team!

You will demonstrate, minimum 4-5+ years experience external monitoring of commercial studies in Oncology. 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 SeniorClinical Research Associate, you will be fully dedicated to one of our global pharmaceutical clients focused on oncology studies. This exclusive partnership offers a culture of innovation, flexibility, and collaboration to bring life-improving treatments to market.

• Full ownership of investigator sites from study initiation to close-out
• Conducting feasibility, site selection, interim, and close-out visits
• Building strong relationships with investigator site staff to meet key clinical metrics
• Attending investigator meetings, ensuring proper shipment, storage, and accountability of clinical supplies
• Monitoring data integrity and compliance with clinical trial guidelines

Qualifications

you will need:

• Solid experience as a Senior CRAwithin a pharmaceutical company or CRO
• Strong expertise in Oncology (other Phase II-III commercial trial experience is also valued)
• Experience in RBM/RBQM (Risk-Based Monitoring & Quality Management)
• Excellent organizational skills and ability to adapt to a dynamic environment
• Strong IT skills and ability to multitask 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 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

#LI-DC1#LI-Hybrid

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

ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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 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