[직무내용]

아이콘 유한회사

아이콘 유한회사(ICON Plc)는 다국적임상시험 수탁기관으로 1990년 아일랜드 더블린에 본사가 설립되어 비지니스를 시작하여, 지난 30년간 글로벌 기업으로 성장하였음.
당사가 설립된 이래 새로운 약물 및 치료법 개발을 통해 환자의 안전과 생명을 구하고, 궁극적으로는 인류 삶의 질을 향상 시킬 수 있는 약물, 치료법 및 의료기기 개발 가속화에 이바지 하는 것을 목표로 하고 있음. 
임상시험 서비스 각 분야의 글로벌 전문가들로 구성된 임직원들이 제약, 생명공학, 의료기기 관련 기업, 학술단체 및 정부기관 등의 고객들에게 전문적이고, 혁신적이며, 종합적인 다국정 임상시험 아웃소싱 및 컨설팅 서비스를 제공해오고 있음. 
2022년 현재, 전 세계 53개국, 119개 지역에 약 40,500 명 이상의 임직원들이 근무하고 있음. 

아이콘클리니컬리서치코리아(유)는 아이콘 유한회사(ICON plc.) 의 한국 지사로 2005년 한국 내 법인이 설립되었음. 서울 강남구 역삼동에 사무실이 위치하고 있으며, 약 700여명의 임직원이 재직중으로, 신약 및 치료법 개발을 위한 임상시험 진행을 위해 필요한 다양한 분야에 서비스를 제공하고 있음.

채용직무
Site Activation Lead (Study Start Up PM)
Home based, Korea
 
The Site Activation Lead is responsible for ensuring the successful and timely activation of investigative sites to ensure that sites are activated in line with the study timelines and client expectation. The Site Activation Lead provides oversight for activities associated with substantial amendments as required. The Site Activation Lead is the functional representative of the Study Start Up department at the project team level.

• Client Relationship:
- Prepare/contribute to client and project specific site activation strategy and site activation plan and work cross-functionally.
- Ensure adequate oversight of project in terms of timely delivery of key timelines and that the impact of missed deliverables is understood by all key stakeholders.
- Attends client calls, where required and ensures that both the interests of the client and of ICON are robustly defended.

• Operations Management:
- Oversees day to day delivery of all aspects of site activation in the projects assigned.
- Ensures that each project has a site activation plan and that the study is being conducted in accordance with that plan and in an effective manner which meets sponsor timelines and expectations and is in compliance with ICON/client KPIs, ICON/client SOPs, reporting norms, appropriate regulations and ICON's quality standards
- Ensure that tasks associated with substantial amendments during the site activation and maintenance phase of the clinical trial 
- Ensure effective resource planning and allaocation within projects assigned.

You will need:
• Bachelors' degree or local equivalent in medicine, science, or equivalent.
• Previous experience in managing studies in the region. 
• Experience in oversight of study deliverables, ideally with proven experience in the oversight of site activation project phase and/or staff in a global/multi-regional environment & familiar with GCP requirements.
• In-depth experience within clinical research with experience in the Clinical studies regulatory environment and a leadership role.
• Excellent written and verbal Communication skills in Korean and English
** Experience in medical devices is a bonus

[근무시간 및 형태]
주 5일 근무
(오전) 9시 00분 ~ (오후) 6시 00분
주소정근로시간 : 40시간


[급여조건]
- 월급 5000000원 이상
- 상여금 : 5% (미 포함)
- 면접 후 결정 가능


[장애인채용희망여부]
장애인 병행채용


[병역특례]
- 비희망

해당 채용 정보 문의하기