Cra I
il y a 1 jour
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.
**The role**:
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. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.
Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
**You will need**:
- University degree in medicine, science, or equivalent
- You should also have knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
- You will possess excellent written and verbal communication in English
- Good social skills enabling you to deal with queries in a timely manner
- You will be asked to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid drivers 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.
-
Cra I
Il y a 3 mois
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...
-
Cra Ii
Il y a 7 mois
Paris, France ICON plc 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...
-
Cra Ii/ Senior Cra
il y a 21 heures
Paris, France ICON Temps plein**CRA II or Senior CRA** **Home or Office Based - France** 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...
-
Cra Ii
il y a 6 jours
Paris, France Icon plc Temps pleinAt 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,...
-
Cra Monitor
il y a 1 semaine
Paris, France Icon plc Temps pleinAt 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,...
-
Cra Ii
il y a 1 jour
Paris, France ICON Temps pleinAt 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,...
-
Senior Clinical Research Associate
Il y a 7 mois
Paris, France ICON Temps pleinWe are looking for motivated, reliable, and dedicated CRAs with at least 3 years of independent external monitoring of commercial studies. Experience in Diabetes/Obesity, Cardiovascular, Chronic Disease, or Rare Diseases, especially in phases I-II-III, is an asset. As a Clinical Research Associate, you will be dedicated to our global pharmaceutical...
-
Assistant(E) de Gestion Administratif(Ve)
Il y a 7 mois
Paris 8e, France Regulation Partners Temps plein**Fiche de poste** **I - DESCRIPTION DU POSTE** **_1 - Intitulé du poste :_** **Assistant(e) de Gestion Administratif(ve)** **BAC + 2 (2 ans d’expérience)** **_2 - Le positionnement du poste dans l’organisation : _**: - _ Sous l’autorité du Responsable des Services Financier et Administratif **II - MISSIONS ET ATTRIBUTIONS** **_1 - Tâches...
-
Logistics Coordinator I
il y a 1 semaine
Paris, France Icon plc Temps pleinAt 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,...
-
Clinical Research Associate
Il y a 7 mois
Paris, France Institut de Myologie Temps pleinLocated in Paris at the heart of Europe’s largest hospital, the Pitié-Salpêtrière, the Institute of Myology was created in 1996 under the impetus of an association of patients and parents of patients, the AFM-Telethon. Its objective is to promote the existence, recognition and development of myology as a clinical and scientific discipline in its own...
-
Clinical Research Associate
Il y a 7 mois
Paris, France Icon plc Temps pleinICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical and biotechnology organisations. With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and...
