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CRA II

  1. Paris
2025-116646
  1. Clinical Monitoring
  2. ICON Strategic Solutions
  3. Remote

About the role

 

We 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 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 our exclusive programs.

 


We are currently looking for a Clinical Research Associate to join one of our sponsor-dedicated teams in Issy-les-Moulineaux (1-2 days office based).

 

Key responsibilities include: 

  • 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

 


You will need:

  • A first stable experience as a CRA, this within the pharmaceutical industry or a CRO (min 1 year)
  • 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

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.

List #1

Day in the life

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How to excel as a CRA in a Clinical Research Organisation

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Our People

Content type

Blogs

Publish date

08/29/2023

Summary

To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

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Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

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Progressing as a CRA with ICON

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Publish date

05/23/2023

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How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce

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 Senior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.

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Suzaita's story - an insight into working in Clinical Research

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04/05/2023

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Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfilled?

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Senior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.

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