핵심 정보
- 경력
- 경력 7년 ↑
- 학력
- 대졸(4년제) 이상
- 근무형태
- 정규직 수습기간 3개월
- 우대사항
-
- 외국어 능력영어능통자
- 활동/경험해당직무 근무경험
- 급여
- 면접 후 결정
- 근무지역
- 서울 용산구
본 채용정보는 마감되었습니다.
(주)한국얀센에서 채용공고가 시작되면 이메일로 알려드립니다.
상세요강
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where
complex diseases are prevented, treated, and cured, where treatments are
smarter and less invasive, and solutions are personal. Through our expertise in
pharmaceutical, medical devices and diagnostics markets, we are uniquely
positioned to innovate across the full spectrum of healthcare solutions today
to deliver the breakthroughs of tomorrow, and profoundly impact health for
humanity.
Learn more at https://www.jnj.com/.
1. 포지션:
MAF - Therapeutic Area Lead - Immunology
2. 계열사: 한국얀센
3. 근무지: 서울시 용산구
4. 근무 형태: Regular
[Summary]
Lead
the development and implementation of the medical strategy and plan of the
assigned therapeutic area, including integrated evidence generation plan (IEGP)
and TA IVT strategy, via close collaboration with internal/external
stakeholders and alignment with the global/regional TA medical strategy as well
as TA business strategy. and review medical/ promotional materials within
assigned therapeutic areas [Medical Advisor/Therapeutic Area Lead]
Be
responsible to review study proposals and reports/manuscripts from Company
sponsored studies to investigator-initiated studies [Study Responsible
Physician/Scientist]
Define
MSL strategy aligned with brand strategy based on generated medical insights
and Lead MSLs to ensure full implementation of medical plans by coaching and
supporting [MSL Manager]
[Main responsibilities]
Medical
Advisor/Therapeutic Area Lead for assigned TAs
Act
as a Medical Affairs Expert and lead the development and implementation of the
medical strategy for a specific product (group of products) or franchises
•
Develop
and maintain deep knowledge in products, market trends, competitor activities
etc.
•
Develop
Medical/Brand strategies aligned with company strategy
Provide
expert medical leadership for other internal functions (Medical, Commercial,
Regulatory affairs, Market Access etc.)
•
Provide
consultation to Medical Information for the assigned therapeutic areas
•
Provide
expert medical leadership into issue management (e.g. product withdrawals,
safety alerts etc.)
•
Provide
input to business development initiatives for allocated product(s). When
requested Partner with the late lifecycle management group to provide proactive
medical input for lifecycle extension opportunities as appropriate
•
Act
as a medical representative in meeting with government affairs, such as HIRA
and MFDS upon a request of regulatory affairs or market access
Lead
integrated evidence generation plan (IEGP) process with TA cross function teams
•
Lead
local IEGP discussion to identify the data gaps and KRQs required to support
the short-term and long-term TA medical/business strategy
•
Represent
Country and promote local data/clinical gaps found from IEGP and KRQs to
regional TA IVT (Integrated Value Team)
Build-up
and maintain External Relationships
•
Build
up or enhance a trusted collaboration with the external scientific community in
order to facilitate a continuous communication and transfer of knowledge, from
key opinion leaders and a wider group of physicians and customers.
•
Leverage
relationships with investigators and key opinion leaders to gain input into the
development of the product strategy and to specific protocols.
Coach
and support Medical Events
•
For
Medical Education activities, support the MSL/Medical Advisor on Medical
Education programs concept, review the program proposals and final program
outline and support the review of scientific Medical Education materials
•
For
medical consulting events including Advisory Board Meetings or consulting with
KOLs, Lead or support the MSL/Medical Advisor on generating Key business
questions, selecting relevant HCPs with reviewing proposals and final outlines
and review of scientific materials
Support
and review science of company materials
•
Review
promotional materials with ensuring brand messages relating to allocated
product(s) (including core medical education materials, abstracts, medical
information materials, marketing materials etc.) accurately reflect scientific
data and are fully compliant with applicable regulations.
•
Support
and review Materials for patient support/education and for Medical Affairs
(slide decks, Q&A...)
Collaborate
with other regional/countries (Medical/Regulatory Affairs, Market Access in
North Asia/Asia Pacific)
•
Work
with AP teams to gather local inputs and to drive alignment of strategy/plan
for the assigned product plan(s) for designated TAs
•
Act
as a co-lead of the Integrated Value Team (IVT)
•
Deliver
medical insight into Product Life Cycle Management planning especially for
locally developed product when it is applicable.
Study
planning and Execution [Study
Responsible Physician/Scientist]
Investigator-Initiated
Study (IIS)
•
Support Medical Affairs to evaluate proposals
of IISs for scientific soundness and whether those are in alignment with the
medical strategy.
•
Work with and
support Clinical Research team and GCO -MAO team in the oversight of IISs
Local
Company-Sponsored Study (CSS)
•
Support the development of country specific
study proposals for post registration local studies
•
Participate in study planning, e.g., with
respect to evaluation of local business needs, timelines, grants and
investigator/ site selection
•
Participate in study start-up meetings and
other activities to provide the appropriate training and information to
investigators and site personnel.
•
Support Clinical Operations, when needed, to
address any questions and/or clarify issues arising during the conduct of
studies.
Global
Development Program
•
Provide local country feasibilities for global
R&D programs, such as epidemiology, current clinical practice, on-going
competitor studies etc. upon a request of GCO
•
Recommend relevant investigator sites
considering available patient pools, site capabilities and future company
business plans
•
Visit investigators for boosting enrollment,
issue management etc. upon a request
Publication
•
Support the development and implementation of
the publication plan at local level.
•
Review and approval manuscripts
•
Support efforts that ensure that J&J guidelines
for publication of studies are followed, and that all MAF studies are published
in accordance with J&J policy.
MSL Manager
Define MSL strategy within Medical
Affairs and Lead MSLs to ensure full implementation of the Medical Plans
Strengthen external customer management
in the field by building up the capability and capacity of MSLs to ensure high
quality scientific engagement
Coach MSLs to develop strategic
partnership with internal stakeholders via generated medical insights
Enhance the cross-functional
collaboration between MSLs and all stakeholders.
Ensure strict medical compliance in MSL
daily activities.
Coach and support individual MSL for best
performance and career development.
•
Recruit and establish a qualified MSL team
•
Provide continuous coach to MSLs to ensure the
MAF competencies and effectiveness towards team and individual goals
•
Inspire and motivate them by active, open and
constructive communication
•
Coach and support them for desired
A member of MAF leadership team
•
Support the Country Medical Director in the
execution and supervision of all country Medical activities
Compliance
•
Ensure safety reporting requirements (timely
AE/PQC reporting) as set out in company policies and SOP’s (Standard Operating
Procedures) are met and appropriately managed when planning projects,
developing materials, executing projects and contracting vendors;
•
Ensure relevant quality, medical, HCC and
legal compliance requirements are fully understood, appropriately managed and
complied with when planning projects, developing materials, executing projects
and contracting vendors.
[Qualifications:]
Education: Advanced
degree in Master of science and above (PhD, MD, or PharmD) is preferred with a
major of pharmacy, medical or life science, Medical Doctor is preferred
Related experience:
•
At least 2-3 years’ experience in clinical
practice or at least 7 years’ experience in pharmaceutical industry is preferred.
•
Understanding of local regulatory policy and
industry’s code of practice related to drug registration, pharmaceutical promotion,
and clinical study.
Job specific competencies/skills required:
•
In-depth scientific and/or therapeutic knowledge,
strength in research and interpretation of scientific publications
•
Knowledge for research, clinical trial design and process
•
Knowledge of national healthcare and access system
•
Excellent English language skills, spoken and written
•
Interpersonal and communication skills to effectively
interact with a broad range of external and internal personnel.
•
Must be familiar with Microsoft Word, Excel and
PowerPoint
•
Awareness of, and adherence to, Johnson & Johnson
Credo values and International Health Care Business Integrity Guide
The role
involves extensive interactions with:
•
Externally, Health Care Professionals
•
Externally, Academic Society
•
Health Care Compliance/ Legal
•
Brand team in local/regional operation
•
Regulatory Affairs and Market Access in local and regional
operation
•
Global Clinical Operation/ Medical Affairs Operation
(GCO/MAO)
•
All Medical Team leaders and members in
local/regional/global operating teams
[JD 확인 및 지원 방법]
www.careers.jnj.com -> Requisition number “2406185393W”검색 -> 해당 모집 공고 클릭 후, “Apply Now”
[제출 서류]
영문 자유 양식의 이력서/경력술서/자기소개서
[서류 마감일]
채용시 마감
[유의사항]
- 국가보훈 대상자 및 장애인은 관련 서류 제출 시 관계
법령에 의거하여 우대합니다.
- 서류 전형 합격자에 한하여 개별 통보합니다. 단, 회사 사정에 따라 지연될 수 있습니다.
- 입사 지원 서류에 허위 사실이 발견될 경우, 채용 확정 이후라도 채용이 취소될 수 있으며 향후 채용이 제한됩니다.
- 제출된 서류는 반환되지 않으며, 별도 요청 시 삭제합니다.
www.careers.jnj.com
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