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At IQVIA™, we know that meaningful results require not only the right approach but also the right people. Regardless of your role, you’ll have the opportunity to play an important part in helping...
22 hours ago - Source neuvoo-b
Job Description Parexel is in the business of improving the world’s health.We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific...
22 hours ago - Source neuvoo-b
Job Description We are recruiting for a Regulatory Affairs Associate to join our Clinical Trial Regulatory Services EU Consulting team in Ukraine.This is an ideal role for someone who would excel...
23 hours ago - Source neuvoo-b
Here at Syneos Health we are currently recruiting for a CRA I in CNS department. The Clinical Research Associate I (CRA I) will perform monitoring and site management activities for Phase I-IV...
23 hours ago - Source neuvoo-b
Dear candidates! Please, apply with CV in English only. Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients...
23 hours ago - Source neuvoo-b
The CRA is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with AZ Procedural Documents…
1 day ago - Source indeed
Good knowledge of study set up, site initiation, or study start up experience or equivalent clinical operations experience working in a clinical research…
3 days ago - Source indeed
Basic understanding of clinical research principles and process. Clinical Research Associate / Sr. CRA in Ukraine (Kyiv or Kharkov) with CNS, Schizophrenia TAs…
1 month ago - Source indeed
Medpace is a full-service clinical contract research organization (CRO). Assessing the clinical research site’s patient recruitment and retention success and…
1 month ago - Source indeed
Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
30 days ago - Source indeed
We provide clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries, assisting with key product…
2 months ago - Source indeed
Strong knowledge of GCP and local laws and regulations for clinical trials. Perform clinical on-site monitoring activities (source data verification and review,…
5 months ago - Source indeed
You have previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits).
3 days ago - Source indeed
Oversight and interaction with clinical research sites; Review of patient charts and clinical research data; and. University degree in health-related field;
3 months ago - Source indeed
Excellent understanding and working knowledge of clinical research, phases of clinical trials,. Current GCP/ICH & country clinical research law & guidelines.
10 months ago - Source indeed
Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions…
2 months ago - Source indeed
You have previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits).
2 months ago - Source indeed
Basic understanding of clinical research principles and process. Clinical Research Associate is responsible for site qualification, initiation, interim…
3 months ago - Source indeed
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