MEDPACE에서는 사세 확장에 따라 아래와 같이Clinical Research Associate를 채용합니다.

MEDPACE 는 미국에 설립된 Global CRO로 본사는 미국 Cincinnati에 있으며 North/South America, Europe, Asia, the Middle East, Australia, Africa등 대부분의 국가에 지사를 두고 있습니다.

MEDPACE 한국 지사는 2012년 한국에 설립된 이후 현재까지 다양한 영역에서 Global 과제들을 전문적으로 수행하고 있습니다. 입사시 직원들에게 충분한 training기간을 통해 업무와 회사 생활에 적응할 수 있도록 지원하고 있으며, work & life balance를 통해 직원과 회사가 상생하는 것을 지향하고 있습니다.

관심있는 여러분의 많은 지원을 바랍니다.

Clinical Research Associate

Responsibilities

- Verify that the rights and well-being of subjects are protected, the reported trial data are accurate, complete, and verifiable from source documents, and the conduct of the trial is in compliance with the currently approved protocol/amendment(s), GCP, and applicable regulatory requirement(s);

- Ensure site compliance while conducting qualification, study initiation, routine monitoring, and study site close-out visits for research sites according to Medpace/Sponsor Standard Operating Procedures (SOPs);

- Serve as the primary resource to the clinical investigator and site staff;

- Maintain close collaboration, interaction, and effective working relationships with Medpace internal cross-functional teams; and

- Ensure quality completion of visit reports, follow-up letters, and maintenance of study-related databases and ClinTrak ® Monitoring Portal.

단체 상해보험/ 유연근무제/ 재택근무가능/ 명절상품권지급/ 경조휴가/ 휴대폰비용지원

Qualifications

- Bachelor's degree in a health or science related field and with at least 1.5 to 5 years of experience in clinical monitoring;

- Comprehensive knowledge of practices and procedures relating to all clinical monitoring visit types, including practical application of this knowledge;

- Demonstrated ability to act as a Lead CRA (as applicable);

Act as a resource for new CRAs and ability to facilitate training and serve as a mentor for new CRAs; and

- Implements new ideas/solutions, without prompting, within their authority.

지원방법 : Email (SouthKoreaHR@medpace.com)로 영문이력서 (MS Word or PDF) 및 문의사항 발송

공고 관련 문의 : M.LauMeiSze@medpace.com