CRA II or Senior CRA

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

Offer summary

Qualifications:

Bachelor's degree in a scientific or healthcare-related field., Minimum of 2 years of experience as a Clinical Research Associate., In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines., Strong organizational and communication skills, with attention to detail..

Key responsibilities:

  • Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborate with investigators and site staff to facilitate smooth study conduct.
  • Perform data review and resolve queries to maintain high-quality clinical data.

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ICON plc XLarge http://www.iconplc.com
10001 Employees
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Job description

CRA II or Senior CRA, home based, Turkey

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

We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies

What you will be doing

Required profile

Experience

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

Other Skills

  • Verbal Communication Skills
  • Organizational Skills
  • Detail Oriented
  • Collaboration

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