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Clinical Research Associate Cro Jobs in Georgia (NOW HIRING)

Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical operations professional responsible for managing site monitoring and relationship activities across multiple clinical ...

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Clinical Research Associate Cro information

What is the difference between Clinical Research Associate Cro vs Clinical Trial Assistant?

AspectClinical Research Associate CroClinical Trial Assistant
CredentialsBachelor's degree, often with certifications like CCRP or RACTypically a high school diploma or associate degree, with some roles requiring a certificate
Work EnvironmentConducts site visits, monitors trials, and ensures complianceSupports trial coordination, manages documentation, and assists with logistics
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, CROs, clinical trial teams

The Clinical Research Associate Cro focuses on monitoring clinical trials, ensuring compliance, and site management. In contrast, the Clinical Trial Assistant provides administrative support, manages documentation, and assists with trial logistics. Both roles are essential in clinical research but differ in responsibilities and required experience.

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Infographic showing various Clinical Research Associate Cro job openings in Georgia as of June 2026, with employment types broken down into 1% As Needed, 84% Full Time, 6% Part Time, 1% Temporary, and 8% Contract. Highlights an 72% Physical, 3% Hybrid, and 25% Remote job distribution.

Clinical Research Associate

Atlanta, GA • On-site

Other

Posted 28 days ago


Job description

HungaroTrial is the largest regional CRO in Central and Eastern Europe with 10 offices in the region and USA, plus Business Development office in London, UK. Due to the expansion of our operations in the USA we are looking for CRA colleagues with at least 2 years of active monitoring experience.


As a Clinical Research Associate you will be responsible for a variety of monitoring tasks and you will have a chance to work on clinical studies in different therapeutic indications, ensuring the clinical trial is conducted in compliance with study protocol and procedures, ICH-GCP guidelines and the applicable regulations and SOPs.


Main duties and responsibilities

  • Initiate, monitor and close-out clinical studies on study sites in accordance with applicable regulations, guidelines of ICH-GCP and standard operation procedures;
  • Prepare and perform regulatory and ethics submission (drug, medical device, non-interventional) for approval in accordance with applicable regulations, guidelines of ICH GCP and standard operation procedures of HungaroTrial (e.g. able to perform initial CA and EC submissions, amendment, notification, progress and safety report submissions, contract negotiations without direct supervision);
  • Supportcontracting procedure between Sponsor and Investigational sites;
  • Perform feasibilities and pre-study evaluations;
  • Document activity in accordance with ICH-GCP and standard operation procedures of HungaroTrial;
  • Prepare a summary (report) of activities as requested by the Manager.


Requirements

  • Bachelor degree in life sciences
  • at least 2 years experience in CRA role
  • experience in Oncology clinical trials
  • native level of English
  • Confident IT skills
  • Driver’s license
  • effective communication, customer focus, teamwork, time management, motivation to learn and develop


What we can offer

  • Attractive and competitive salary
  • Dedicated and supportive team
  • Multinational environment
  • Regular team buildings and company events


We take special attention to the balance of the work and your private life.