Senior CRA

Pharmaceutical Research Associates, Inc; France; À distance; EUR 40 000 - 60 000; Plein temps

Résumé du poste

Une entreprise de recherche clinique recherche un Clinical Research Associate pour superviser les sites d'études. Ce rôle implique une gestion complète des sites, des visites de sélection et un suivi proactif, en collaboration avec des clients pharmaceutiques de premier plan. Rejoignez une équipe dynamique axée sur l'innovation et le développement de médicaments.

Prestations

Assurance santé

Programmes de retraite compétitifs

Assistance aux employés

Congés annuels variés

Avantages flexibles

Qualifications

• Expérience stable en tant que CRA dans l'industrie pharmaceutique ou un CRO.
• Compétences organisationnelles excellentes.
• Fluent en français et professionnel en anglais.

Responsabilités

• Gestion complète des sites d'investigateurs pour les études assignées.
• Visites de site pour la sélection et le suivi.
• Maintien de l'intégrité des données cliniques.

Connaissances

Organisation

Communication

Multitâche

IT

Description du poste

Overview

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.

Responsibilities

As a CRA 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 CRAs based in France area to join our dedicated CRA team! You will demonstrate, ideally at least 15 months independent external monitoring of commercial studies in Oncology. Other therapeutic areas are also of interest, especially if gained on phase II, III commercial trials.

• What you will be doing:

  As a Clinical Research Associate, 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.

  • 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.

Qualifications

you will need:

• A first stable 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.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-Remote

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