Clinical Operations Assistant

최소 1년 이상 CTA (Clinical Trial Assistant) 혹은 관련된 Admin 경험 보유자

또는

최소 1년 이상 Study Coordinator 경험 보유자

경력에 따라 Sr. 레벨로 채용 예정

생명과학, 화학, 간호학, 약학 전공자

공인영어성적 소유자

지원 시 제출 서류: 공인영어성적표, 학부 성적표

Descriptions

• The role of the Clinical Operations Assistant (COA) is to maintain the paper and electronic Central Files for Clinical Operation, ensuring efficiency, accuracy and quality. Depending on the location of the role may include the tracking, scanning, filing, entry and return of Case Report Forms to clients for assigned projects, upload and naming of documents to the electronic document management system, EDC User Management activities and activities associated with Impact Harmony, as appropriate. COA is also to support all site management team members on local billable administrative tasks and assist with QC of Central files.
• Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word.
• Maintain a basic knowledge and ensure compliance with applicable ICH-GCP Guidelines, international and local regulations and applicable PAREXEL procedures.

Skills Requirements

• Good oral and written communication skills to internal and external customer.
• Ability to prioritize multiple tasks and achieve project timeline.
• High commitment to and performs consistently high quality work.
• Good written English skills