Clinical Research Associate - Austria (GCP Monitoring)
Syneos Health Inc
Syneos Health is seeking a Clinical Research Associate (CRA) in Austria. In this role, you will manage site qualifications, ensuring compliance with ICH-GCP and relevant protocols while handling regulatory responsibilities. Successful candidates will possess a Bachelor’s degree or RN and previous monitoring experience in Austria, along with fluency in both German and English. Up to 75% travel is required. #J-18808-Ljbffr
$70.1k - $126.1k
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$115k - $125k
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$71.9k - $189k
...Clinical Research Associate, Sponsor Dedicated Location: Gloucester, United States of America | Full... ...located. Essential Functions Perform site monitoring visits (selection, initiation,... ...ISF) is maintained in accordance with GCP and local regulatory requirements. Create...Full timePart timeLocal areaImmediate start- ...The Clinical Research Associate (CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety... ...prevailing laws, Good Clinical Practices (GCP), and the Sponsor's standards. The CRA is accountable...Local areaRemote work
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$91.34k - $114.17k
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$71.9k - $169.3k
...with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates... ...We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key... ...scope of work, Good Clinical Practice (GCP), and ICH guidelines. Collaborate...Full timePart timeImmediate startWorldwide- ...Summary In this Clinical Research Associate role (may be contract or full‑time employee), you will be responsible for monitoring the progress of clinical studies, either at investigative sites... ...operating procedures (SOPs), ICH‑GCP, and all applicable regulatory requirements...Full timeContract workInterim roleLocal areaRemote work
$125k - $145k
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