공통 자격요건 | [지원자격] - Education-Scientific and/or Medical
background
- Experience & knowledge -
Pharmaceutical experience is preferred
- Good verbal and written English
knowledge and skill
- Understanding in pharmaceutical
environment, regulation and business
- Excellent communication skill
- Negotiation/influencing skill
- Finance awareness & judgement |
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Medical Operations Specialist 0명 | [근무회사] * 근무회사: 고속터미널역에 위치한 프랑스계 글로벌 제약회사 * 사업분야: 전문 의약품, 헬스케어, 백신, 의료기기 등 * 모집부서: SG Medical * Position Title: Medical Operations (MO) * 특이사항: 재택근무, 중식, 초과근무
수당 별도 제공
[회사소개] - 프랑스에 본사를
둔 세계 선두의 헬스케어 기업으로, 국내에서는 전문의약품 및 건강기능식품을 공급하고 있으며, 이 외에도 백신, 희귀질환치료제를 통해 예방에서 치료까지, 환자들의 다양한 니즈에 부응하는 통합적인 헬스케어 기업으로 자리매김하고 있습니다. [업무내용] * 경력에 따라 업무 조율이 발생할 예정입니다. 신입도 지원 가능한 포지션이니 많은 관심 부탁드립니다.
Job Purpose : 1. To contribute to the accomplishment of
Medical strategies by planning, managing and conducting clinical trials in
accordance with regulatory and ethical standards. 2. To develop plans and contribute
carrying out the strategic activities in accordance with global medical teams
and local medical teams. 3. To coordinate to execute scientific
engagements (congress & events), scientific communications, scientific
education and scientific publications.
Key Accountability 1. Provide the operational excellence in
the planning and execution of clinical studies as the medical point of contact
in partnership with Clinical Study Unit(CSU). (1) Coordinate to develop and approve the
study outline and protocol in accordance with brand strategy. (2) Carry out study start up activities
(country/study/site feasibility, investigator meeting, contracting etc.) in
case of necessity. (3) Monitor study progress until CSR
completion (timeline, resource allocation, etc.) (4) Resolute study operational issues and
develop mitigation plans reflecting medical perspectives. (5) Ensure data accuracy in tracking
system. (6) Ensure investigational product
supply.
2. Manage and establish the operational
excellence in medical program (e.g. Managed access program)
3. Ensure timely execution of publication
plans and support internal/external stakeholders for any process related to
publication.
4. Manage the medical budget including
trial and non-trial data tracking and accurate reporting.
5. Ensure timely execution of medical
education plans, scientific insight generation, stakeholder mapping and
segmentation in line with medical strategy.
6. Provide country oversight and
governance of regulatory, compliance and transparency reporting requirements
for medical activities.
7. Develop country scientific curricula
and content strategies to support successful launches capitalizing on multiple
digital platforms.
8. Develop and manage required documents
using appropriate internal system(e.g. e-BUY, NAYA, e-approval, e-VMF,
e-expense, myTransparency etc.).
9. Communicate with internal /external
stakeholders to manage clinical trials and scientific programs.
10. Develop internal documents (e.g. SOP,
working guideline, process map, etc) in case of necessity.
[전형절차] - 서류심사 > 1차 면접 > 2차 면접 > 합격 * 절차의 경우 업체
상황에 따른 변동이 있을 수 있습니다. |
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