채용정보

(주)글락소스미스클라인

조회수 1631

PMS Lead (Fixed-term)

  • 계약직(12개월)
  • 경력(5년 이상)
  • 대졸(4년제)
  • 직종
    제약·산업 임상허가
  • 급여
    로그인 후 확인 가능
  • 고용형태
    로그인 후 확인 가능
  • 모집인원
    1명
  • 근무지역
    서울 용산구
  • 학력
    대졸(4년제)
  • 접수마감
    채용시

모집부문 및 자격요건

  • 모집부문
    제약·산업 임상허가
  • 담당업무
    PMS Lead
  • 자격요건
    경력(5년 이상)
    대졸(4년제)

세부사항

확대세부사항을 확대할 수 있습니다.

계약기간은 1년 계약 후 성과에 따라 최대 2년까지 근무 가능합니다.


Job Purpose

Manages all aspects of long-term and/or multi-center regulatory research projects, including planning, coordination, execution, outsourcing, and risk management, ensuring compliance with written standards, local legislation, licensing conditions, and regulatory requirements.

 

Key Responsibilities

Responsible for overseeing regulatory commitment studies, ensuring full compliance throughout the project lifecycle, including data collection, analysis, and report writing, in accordance with regulatory requirements.

Ability to develop and manage key study documents, ensuring alignment with scientific evidence and compliance with written standards and mandatory regulations.

Take business ownership of relevant vendors, conducting oversight and risk management in alignment with GSK’s Internal Control Framework (ICF).

Collaborate effectively with team members and key stakeholders to ensure successful project execution.

Perform any other assignments as directed

 

Requirements

BS in science or related field (Pharmacy, nursing, biology, epidemiology, life sciences)

6~8 years related experience (Study project management

Protocol, CRF, SAP development, CRO outsourced resource & contract management from vender assessment to execution, Budget projection & finance management, MFDS engagement, Hospital/clinical experience, Audit and clinical quality)

Experience working in the pharmaceutical industry, collaborating with operational teams to better understand requirements and applying solutions efficiently.

Maintain a high level of integrity while managing multiple priorities and responsibilities with a strong attention to detail and strategic organizational skills.

Focused on solution-oriented thinking, agile in adapting to new systems and processes, and motivated to work with new applications and business processes.

Demonstrate excellent verbal and written communication skills, with the ability to engage effectively with all levels both internally and externally, and the ability to write clear technical documentation required by regulatory agency (MFDS) in accordance with internal policies and national legislation.

Demonstrate a strong commitment to accuracy, quality, and meeting goals or deadlines, with a sense of urgency, flexibility, and accountability. Must be a committed active team player, prepared to work in and embrace a collaborative, team-based culture, while providing expertise to train site personnel.

Experience as the first author or co-author in research papers is highly valued. Include citation links to relevant publications in your CV

Native Korean/business level of English

근무조건

  • 급여조건
    로그인 후 확인 가능
  • 고용형태
    로그인 후 확인 가능
  • 근무형태
    로그인 후 확인 가능
  • 근무지역
    서울 용산구 한강대로 92 (한강로2가, LS용산타워) 9층
  • 근무요일
    주5일
  • 근무시간
    재택혼합 및 유연근무

접수방법 및 채용절차

  • 등록일
    01.24(금)
  • 마감일
    채용시
  • 접수방법
    로그인 후 확인 가능
  • 전형절차
    서류전형1차 면접최종 합격
  • 제출서류
    합격 후 안내
  • 담당자명
    로그인 후 확인 가능
  • 담당자 이메일
    로그인 후 확인 가능
  • 담당자 연락처
    로그인 후 확인 가능
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기업정보

데일리팜
(주)글락소스미스클라인
  • 기업분류
    제약·바이오 다국적제약
  • 대표자명
    Borgatta Maurizio antonio
  • 사원수
    -
  • 설립일
    1968년 02월 23일
  • 주소
    서울 용산구 한강대로 92 (한강로2가, LS용산타워) 9층
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