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
Please send CV: 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)).