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Clinical Research Associate - All levels

  1. Argentina
2024-115812
  1. Clinical Monitoring
  2. ICON Strategic Solutions
  3. Remote
  1. Argentina
2024-115812
  1. Clinical Monitoring
  2. ICON Strategic Solutions
  3. Remote

About the role

The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements.


Main activities

  • Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs and study processes.
  • Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations.
  • Ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations and SOPs.
  • Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate.
  • Participates in audit preparation and follow-up activities as needed.
  • May serve as preceptor, providing training to less experienced clinical team members.

Requisitions

 

• Bachelor’s degree in a health, life sciences or medical fields. Completed graduation. 
• At least 3 year of experience with on-site monitoring, preferably with oncology protocols.
• Full availability to travel.
• Fuent English and Spanish (read, write and speak).

Experienced candidates must be based in CABA.

 


What ICON can offer you:

At ICON, inclusion & belonging are fundamental to our culture and values.   We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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.

List #1

Day in the life

A picture of Debora Oh
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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A picture of Yemi Moses
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 excell

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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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A Day In The Life

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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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