Job Overview
Under moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements  at the regional, or country level.
Prepares and manages site documentation; reviews and negotiates site  documents and contracts with sites and sponsors; maintains, reviews, and reports on site performance metrics; serves as the primary point of contact for investigative sites; tracks completion of appropriate documents for sites; ensures contracts are fully executed; and establishes project timelines.  With moderate oversight and supervision, perform tasks at a country/region level associated with site activation activities in accordance with  applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.

Essential Functions
• With moderate oversight and supervision, a Single Point of Contact (SPOC) to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the  Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.
• Prepare site documents, reviewing for completeness and accuracy.
• Inform team members of completion of regulatory contractual. and other documents for individual sites.
• Distribute completed documents to sites and internal project team members.
• Update and maintain internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.
• Review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education.

Qualifications

•  계약직 포지션(6 months)

•  IRB submission 경험자

채용 전형

- 이력서 접수 > 서류전형/Pre-screening > 면접전형 > 최종합격 > 입사

- 지원 방법 : 영문 CV를 첨부하여 본 공고를 통해 지원 (이력서 양식 자율)

- Pre-screening 전형 :

- 면접은 화상 혹은 대면으로 진행되며, 지원자 가능 일시에 맞추어 조율됩니다.

- 각 전형 결과는 합격/불합격 여부와 관계없이 모든 지원자에게 안내됩니다.

- 국가등록장애인 및 국가보훈 대상자는 관련법에 의거하여 우대됩니다.

- 지원서 내용이 사실과 다른 경우 합격이 취소될 수 있습니다.

추천 영상
1. What does it mean to be IQVIAN?

https://youtu.be/dhrtkSGsej4

2. 아이큐비아ㅣ나만 몰랐던 (진짜) 포브스 선정 '세계 최고의 직장'

https://youtu.be/i8hNY49LzPs?si=Zzp2IoY4cqsD2x_e

관련 문의

한국 아이큐비아 채용(IQVIA) 카카오톡 채널을 통해 1:1 문의 하실 수 있습니다.

http://pf.kakao.com/_XeVFs

*채널을 추가하시면 매월 신규 포지션 알림 및 회사 소식을 받아보실 수 있습니다.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com