HungaroTrial CRO
Direct message the job poster from HungaroTrial CRO
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 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. Seniority level
Associate Employment type
Full‑time Job function
Research, Science, and Administrative Industries
Research Services
#J-18808-Ljbffr
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 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. Seniority level
Associate Employment type
Full‑time Job function
Research, Science, and Administrative Industries
Research Services
#J-18808-Ljbffr