Description

Johnson & Johnson is the world's most comprehensive and broadly based healthcare Company, touching the lives of nearly a billion people every day. Our Family of Companies throughout the world compete in consumer, pharmaceutical, and medical devices and diagnostics markets and have the skills and resources to tackle the world's most pressing health issues.

1. 포지션: Associate PV Manager
2. 계열사: 한국얀센 (Janssen)
3. 근무지: 서울시 용산구
4. 근무 형태: Regular

[Summary]

• Ensuring that the LOC Safety activities, related to medicinal products are managed in compliance with local regulations and company policies/procedures at local, regional, and global levels and in accordance with any Product vigilance agreements with third-party business partners
• Having appropriate Pharmaco vigilance and Risk management systems in place in order to assure appropriate oversight for products within its responsibility
• Ensure the pro-active Benefit Risk Management throughout the product life cycle translating global safety data to insights and actions tailoring to local specificities and needs. Support activities related to safety reporting requirements as required by Marketing Authorization Holders (MAH) and/or study sponsors, as applicable.

[Responsibilities]

• Ensure that systems and processes are available for the collection and reporting of safety information to meet local and global requirements
• Maintain oversight on day-to-day AE inbound and outbound reporting as applicable
• Oversee data-generating activities to ensure appropriate review and reporting processes are included in project documents for reporting potential AEs (e.g. patient support programs, market research surveys, internet sites),
• Ensure that day-to-day PV functions are performed satisfactorily and that optimal regulatory compliance is maintained at the LOC level.
• Maintain overall responsibility for the coordination of safety requirements as delegated by Marketing Authorization Holders (MAH).
• Act as the local PV contact person for local PV audit and inspection.
• Ensure awareness of changes in regulations that may have an impact on vigilance activities and responsibilities. Evaluate the impact on local processes and inform the appropriate global and regional groups
• Ensure adequate local signal detection process if required and ensure reporting of potential single case signals or clusters of similar events seen in case processing
• Oversee the full product portfolio, and link with local management and key stakeholders.

Risk Management:

• Have an appropriate system and Risk Management in place in order to assure appropriate oversight for products within its responsibility
• Review and complete country specific Annex as required according to local requirements, if applicable
• Collaborate with Medical Affairs and Regulatory Affairs team to ensure that RMP activities are completed in a timely manner
• Ensure implementation and tracking of RMP activities are in place including documentation of completed activities
• Review all risk management plans and PSURs to obtain information on the risk/benefit profile of products
• Provide Medical Safety input in the pre-authorization phase/submission-planning phase of the product lifecycle to guide appropriate planning and management of RMP-related activities.

[Requirements]

• More than 6~8 years of experience in PV/Medical safety related field essential; experience working in the pharmaceutical industry is strongly preferred
• Experience in conducting training
• Knowledge of PV regulations
• Experience using a global safety database is desirable
• Demonstrated attention to detail
• Excellent written and spoken communication and presentation skills
• Effective decision maker with the ability to assess the impact of actions taken locally on the global PV system
• Fluency in written and oral English in order to facilitate communications with GMO, regional Medical, other global functions, and Health Authority
• High customer orientation
• Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity
• Sound judgment, strong planning, and organizational skills, and the ability to get things done
• Demonstrated a strong sense of urgency
• Strong influencing skills with the ability to explain and defend a position that is in the best interests of patient safety

[지원 방법]
www.careers.jnj.com 접속 -> Position Number 2306130905W 검색 -> 해당 모집 공고의 “Apply Now” 클릭 후 온라인 지원 프로세스 진행

[제출 서류]
영문 자유 양식의 이력서/자기소개서

[서류 마감일]
채용시 마감

[For more Johnson & Johnson]
- J&J Careers 유튜브 채널 : https://www.youtube.com/channel/UCZEsWOZwbcjcXHrgYq7sP4Q
- J&J Korea Facebook: https://www.facebook.com/JNJCareersKorea/
- J&J Linkedin: https://www.linkedin.com/company/johnson-&-johnson/
- J&J Corporate Page: http://www.jobkorea.co.kr/Company/1605233/Info

[유의사항]
- 서류를 MS-Word 나 PDF 로 된 한 개의 파일로 미리 준비 하시기 바랍니다.
- 서류 전형 합격자에 한하여 개별 통보합니다. 단, 회사 사정에 따라 지연 될 수 있습니다.
- 온라인 접수시 “Create Your Account” 를 통해 개인 이메일 계정을 등록하신 후 온라인 지원 프로세스를 진행할 수 있습니다. Ex) G-mail/Naver/Daum 등
- 모집 분야 관련하여 자세한 내용은 J&J 홈페이지에서 확인하시기 바랍니다. www.careers.jnj.com

Qualifications

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