Clinical Research Associate II or Senior CRA

University Positions; Paris; Hybride; EUR 40 000 - 80 000; Plein temps

Résumé du poste

Une entreprise de recherche clinique de premier plan recherche un CRA passionné pour rejoindre son équipe dynamique. Dans ce rôle, vous aurez la responsabilité complète de la gestion des sites d'investigation pour des études cliniques, en veillant à ce que les objectifs cliniques soient atteints. Vous travaillerez en étroite collaboration avec le personnel des sites pour assurer l'intégrité des données cliniques et participerez à des visites de sites variées. Ce poste offre une opportunité unique de contribuer au développement de médicaments qui améliorent la qualité de vie des patients. Si vous êtes motivé par l'impact de votre travail et souhaitez évoluer dans un environnement inclusif et stimulant, cette opportunité est faite pour vous.

Prestations

Plans de santé compétitifs

Bonus annuels

Plans de retraite

Assurance vie

Qualifications

• 18 mois d'expérience en tant que CRA dans des essais de phase I-III.
• Capacité à travailler sous pression et à respecter des délais serrés.

Responsabilités

• Gestion complète des sites d'investigation pour les études assignées.
• Planification et réalisation de visites de sites conformément au plan de surveillance clinique.

Connaissances

Monitoring expérience dans les essais cliniques

Connaissance des directives ICH-GCP

Compétences en communication écrite et verbale

Gestion du temps et respect des délais

Capacité à établir des relations efficaces

Description du poste

Location : Office based (Paris or Lyon) or Home based

Employment Status : Permanent

Department : Global Large Pharma

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.

The role :

• 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.
• Potential to assist in training and mentoring fellow CRAs.

You will be operating as a key part of a global study team and plays a fundamental role in our clients’ drug development processes.

You will need :

• 18 months+ of monitoring experience in phase I-III trials as a CRA.
• Previous monitoring experience in medium-sized studies, including study start-up and close-out.
• Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data.
• Excellent written and verbal communication in English and French language.
• Ability to work to tight deadlines.
• Availability to travel least 60% of the time (international and domestic - fly and drive) and should possess a valid driving license.

Benefits of Working in ICON :

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.

We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.

But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON 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, 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 through the form below.