CRA II

extra holidays - extra parental leave
Work set-up: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Bachelor's degree in a scientific or healthcare-related field., At least 2 years of experience as a Clinical Research Associate., 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.
  • Collaborate with investigators and site staff to facilitate study conduct.
  • Review data 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 early phase w healthy volunteers (homebased near Miami, FL)

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

What you will be doing

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Organizational Skills
  • Detail Oriented
  • Collaboration
  • Communication

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