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Clinical Research Associate

  1. Turkey
2023-104179
  1. Clinical Monitoring
  2. ICON Strategic Solutions

About the role

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ICON plc is a world-leading 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.


As a CRA, you will;

 

  • Serve as a primary contact point between the sponsor and the investigational site.
  • Be assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through to data-base lock.

 

Responsibilities include;

 

  • Site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, monitoring and close-out.
  • Partnering with the CTA, LTM and GTM to ensure overall site management while performing trial related activities for assigned protocols. 
  • May contribute to process improvement and training

Experience required:

  • A minimum of a BA/BS degree is required. A degree in a health or science related field is preferred, however, other relevant experiences and skills may be considered by the hiring manager when considering the candidate’s eligibility.
  • A minimum of 1 year of independent clinical trial monitoring experience is required
  • Good working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines.
  • Good IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home.
  • Proficient in speaking and writing the country language and English. Good written and oral communication skills
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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Our People

Content type

Blogs

Publish date

05/23/2023

Summary

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

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A Day In The Life

Content type

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Publish date

04/05/2023

Summary

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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Suzaita Hipolito

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Suzaita Hipolito

Suzaita Hipolito

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