Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions
• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

• Client Dedicated team, 정규직 포지션

• Require at least 2 years of PMS, OS, Late Phase study or relevant experience.(Oncology or Global study experience is preferred)
• Good English communication skill is required

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.

Life at IQVIA

- 조직 내 다양한 Internal Career Development 의 기회

- Employee Assistance Program (직원 고민 상담 지원 프로그램, 가족 포함)

- 사내 동호회, 팀워크샵, 팀빌딩, 연말파티 등 다양한 Activity 지원

- 다양한 경조 패키지 (경조금/경조휴가/상조용품), 호텔 프로모션/리조트 멤버십 지원

- 명절상여금/생일축하금, 영유아 위탁교육비, 업무용 휴대폰(iphone) 지급

- 재택근무 활성화 및 모바일 오피스, Flexible working hours 운영

- 단체보험 (생명/상해보험, 배우자/자녀 포함) 및 건강검진 패키지 지원

- 연차 외 특별휴가 (Company day, 유급병가) 등

- 직원 추천 보너스 제도

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