We are looking for talented and motivated Clinical Research Associates to join our team.

KEY RESPONSABILITIES INCLUDE:

  • Identify, select, train and initiate appropriate investigational sites for clinical trials
  • To submit clinical trials to RA and EC
  • To monitor and manage the sites to ensure study protocol, SOPs, regulatory and ICH –GCP compliance as well as to ensure the rights and well-being of human subjects are protected and the reported trial data are accurate, complete, and verifiable from source documents
  • To collect and review of essential documents required to study execution
  • To ensure effective resolution of issues identified during the course of the study
    To maintain study files
  • To prepare, collect and review documentation supporting payments for the sites

QUALIFICATIONS AND EXPERIENCE   

  • University degree (medical or biological science degree preferred)
  • Organized and well structured
  • A minimum of 1,5 years of clinical trial monitoring experience is preferred.
  • Strong working knowledge of ICH-GCP and local laws and regulations.
  • Demonstrate the ability to work independently and within the team
  • Expertise in communication, managing multiple priorities and computer literacy
  • Willing to travel
  • Very good English knowledge in speaking and writing

ANY OTHER INFORMATION  

  • Expected to travel up to 60% of working time

CV please send: biuro@actrials.com

Klauzula wyrażenia zgody do przetwarzania danych osobowych do zamieszczenia w CV:

Wyrażam zgodę na przetwarzanie moich danych osobowych dla potrzeb niezbędnych do realizacji procesu tej oraz przyszłych rekrutacji zgodnie z Rozporządzeniem Parlamentu Europejskiego i Rady (UE) 2016/679 z dnia 27 kwietnia 2016 r. w sprawie ochrony osób fizycznych w związku z przetwarzaniem danych osobowych i w sprawie swobodnego przepływu takich danych oraz uchylenia dyrektywy 95/46/WE (RODO)).