Sr. CRA & CRA/±Û·Î¹ú¿Ü±¹°èÁ¦¾àȸ»ç
±Û·Î¹ú ¿Ü±¹°èÁ¦¾àȸ»ç¿¡¼ Site Clinical Research Associate ´ã´çÀںеé(Sr. CRA¿Í CRAºÐ)¸¦ ã°í °è½Ê´Ï´Ù.
- Monitors activities conducted by clinical investigative sites as they relate to company clinical studies to ensure successful execution of the protocol. This position functions in an off-site and affiliate based capacity
- The SCRA conducts clinical site monitoring visits across a maximum of 5 protocols and multiple therapeutic areas, ensuring company studies are conducted according to all applicable regulations and business processes. Ensures regulatory inspection readiness at assigned clinical sites.
- Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and company Standard Operating Procedures (SOPs) and business processes.
- Conducts all clinical site monitoring activities according to the monitoring plan and in accordance with the study timelines and company objectives
- Bachelor¡¯s Degree required; medical/science/nursing background is preferred
- At least 3 years of clinical research monitoring experience. (3 – 5 years).
- Experience in on-site monitoring of investigational drug or device trials is required.
- Good written and verbal communication skills. Written and verbal fluency in English and local language (if not English).
- Oncology experience is highly preferred
- ¾àÇÐ Àü°øÀÚ ¼±È£ÇÕ´Ï´Ù.
´ã´çÀÚ : (ÁÖ)¸¶ÀϽºÅæ¼Ä¡ (www.mstone.co.kr) ¿øÇö¼÷»ó¹« ¿¬¶ôó : 02-2050-0299, 010-8911-5018 À̸ÞÀÏ : hs@mstone.co.kr Áö¿ø½Ã Á¦Ãâ¼·ù : ±¹¿µ¹®À̷¼ °¨»çµå¸®°í, ±Ã±ÝÇϽŠ»çÇ×ÀÌ ÀÖÀ¸½Ã¸é ¾ðÁ¦¶óµµ ¿¬¶ôÁֽñ⠹ٶø´Ï´Ù.
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