Emplois actuels liés à Cra Ii - Paris - Icon plc
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Cra Ii
il y a 1 jour
Paris, France ICON Temps pleinWe are constantly looking for motivated, reliable and dedicated **CRAs who can demonstrate at least 12 months independent external monitoring of commercial studies** (or a mix of commercial clinical studies) ideally in Oncology and Hematology. Other therapeutic areas are also of interest, especially if gained on phase I - II or III commercial trials. **As a...
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CRA II: Observational
il y a 16 heures
Paris, France Fortrea Temps pleinA global company in clinical research is seeking a Clinical Research Associate II (CRA II) for future opportunities in Paris, France. This role involves monitoring observational and registry studies, ensuring compliance with protocols. The ideal candidate will have experience at the CRA II level, strong communication skills in French and English, and be able...
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Cra Ii
il y a 6 jours
Paris, France ICON plc Temps plein**Title: CRA II or Senior CRA** **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...
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Cra Ii
il y a 1 semaine
Paris, France ICON Plc Temps pleinCRA II 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 currently seeking a Clinical Research Associate II Specialist to join our diverse...
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Remote CRA II: Sponsor-Dedicated
il y a 15 heures
Paris, France Syneos Health, Inc. Temps pleinA leading biopharmaceutical solutions organization is hiring a CRA II for a home-based role in Paris. This position involves overseeing clinical research sites, ensuring compliance with regulations, and maintaining high-quality monitoring practices. The ideal candidate will have a bachelor's degree or related qualifications and excellent interpersonal...
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Oncology CRA II – Paris | Remote Monitoring
il y a 14 heures
Paris, France NCBiotech Temps pleinA leading biopharmaceutical organization in Paris seeks a CRA II specializing in Oncology to ensure compliance in clinical studies. The role involves site qualification, management, and thorough documentation to oversee trials effectively. The ideal candidate will possess a Bachelor's degree in a related field, demonstrate good clinical practices, and have...
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CRA II in Oncology
il y a 2 semaines
Paris, Île-de-France サイネオス・ヘルス Temps pleinUpdated: December 16, 2025Location: Paris, 75, FranceJob ID: Not ready to apply?Join our Talent NetworkDescriptionCRA II in Oncology - Multi Sponsor - Based in Paris OfficeSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial...
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Remote CRA II: Training
il y a 16 heures
Paris, France Alimentiv Temps pleinA leading clinical research organization is seeking a Clinical Research Associate (CRA) to support and observe clinical site monitoring services. This role focuses on developing CRA skills while conducting site management activities for studies, ensuring compliance with protocols and regulations. Responsibilities include remote site contacts, data review,...
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CRA II
il y a 2 jours
Paris, France ICON Temps pleinOverviewICON 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 currently seeking a Clinical Research Associate II to join our diverse and dynamic...
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CRA II
il y a 16 heures
Paris, France Syneos Health, Inc. Temps pleinUpdated: December 8, 2025Location: FRA-Paris-HybridJob ID:25103766 Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the...
Cra Ii
il y a 3 semaines
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
As a Clinical Research Associate at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP.
The role:
- Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
- Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
- Balancing sponsor generated queries
- Taking responsibility for study cost efficiency
- Preparation and review of study documentation and feasibility studies for new proposals
- Potential to assist in training and mentoring fellow CRAs
You will need:
- 18 months+ of monitoring experience in phase I-III trials as a CRA
- College degree in medicine, science, or equivalent
- 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
- 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.
