Senior CRA CRA II

extra holidays - extra parental leave
Work set-up: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Bachelor's degree or equivalent in clinical, science, or health-related field., Licensed healthcare professional or equivalent work experience., At least 1 year of clinical monitoring experience for level 2, 3 or more years for level 3., Knowledge of ICH guidelines and local regulatory requirements..

Key responsibilities:

  • Monitor clinical study progress at investigative sites or remotely.
  • Ensure trials are conducted, recorded, and reported according to protocols and regulations.
  • Maintain compliance with SOPs, ICH-GCP, and regulatory standards.
  • Travel up to 70% as required.

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ICON plc XLarge http://www.iconplc.com
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Job description

Senior CRA CRA II

ICON plc is a worldleading 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

Overview:

ICON plc is a worldleading 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.

DESCRIPTION DU POSTE

ICON plc est une organisation de recherche clinique et d’intelligence en soins de santé de premier plan à l’échelle mondiale. De la molécule à la médecine, nous faisons progresser la recherche clinique en offrant des services externalisés aux entreprises pharmaceutiques, biotechnologiques et d’équipement médical, ainsi qu’aux organismes gouvernementaux et de santé publique.

En maintenant nos patients au centre de toutes nos activités, nous aidons à accélérer le développement des médicaments et des dispositifs qui sauvent des vies et améliorent la qualité de vie.

Nos employés sont au cœur de notre culture et constituent la force motrice de notre succès. Les employés d’ICON ont pour mission de réussir et leur passion garantit que nous faisons bien notre travail.

Responsibilities:

As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICHGCP, and all applicable regulatory requirements.

Responsabilités

En tant qu’associé(e) de recherche clinique (ARC), vous surveillerez les progrès des études cliniques aux centres d’étude ou à distance, et vous vous assurerez que les études cliniques sont menées, documentées et signalées conformément au protocole, aux procédures opérationnelles normalisées (PON), aux bonnes pratiques cliniques (BPC) élaborées par la Conférence internationale sur l’harmonisation (CIH) et à toutes les exigences réglementaires applicables.

Qualifications:

What do you need to have?

  • Undergraduate degree or its international equivalent in clinical, science, or health related field from an accredited institution; a licensed healthcare professional (i.e., registered nurse); or equivalent work experience required
  • 1+ years of clinical monitoring experience or equivalent combination of education and experience is required for the level 2 role; 3+ years is required for a level 3
  • ONCOLOGY MONITORING EXPERIENCE PREFERRED
  • ABILITY TO TRAVEL 70%
  • Knowledge of ICH and local regulatory authority regulations regarding drug trials

    • To qualify, applicants must be legally authorized to work in the United States or Canada, and should not require, now or in the future, sponsorship for employment visa status

      Benefits of Working in ICON:
      Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

      At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career both now, and into the future.

      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, 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.

      Qualifications

      Que devezvous avoir?

Required profile

Experience

Level of experience: Senior (5-10 years)
Spoken language(s):
EnglishFrench
Check out the description to know which languages are mandatory.

Other Skills

  • Time Management
  • Teamwork
  • Communication
  • Problem Solving

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