[글로벌 제약사] Medical Science Liaison
Tasks
Join Recordati Korea in Driving Growth
Recordati is a dynamic growing company focused on unlocking the full potential of life. We are constantly looking for highly talent individuals across our business units to help deliver our purpose.
Located in Seoul, Recordati Korea serves as the regional office for all of Asia excluding China and Japan, specializing in rare diseases. We are experiencing rapid expansion, dedicated to swiftly bringing new medications to Korea and the broader Asian market, offering hope to patients with rare diseases. We are seeking proactive, collaborative business professionals to join us in leading our organization forward and growing together.
Position: Medical Science Liaison
Reports To: Country Medical Lead
Areas to look after: Korea
Location: Seoul
Role Purpose
Reporting to the Country Medical Lead, this position leads medical and scientific activities to provide accurate and balanced scientific information to physicians, healthcare professionals, payers, and other external stakeholders, with the aim of supporting appropriate patient access to treatment. This includes facilitating scientific exchange, supporting knowledge dissemination aligned with clinical evidence and guidelines, and contributing to improved disease awareness and diagnosis. The role also ensures full compliance with all relevant internal and external regulations, guidelines, and policies at both local and international levels.
Major Responsibilities
● Scientific Expertise
• Establish themselves as an internal and external product and disease state expert including treatment guidelines, protocols, trends, ongoing and planned studies or own and competitor products.
• Respond in a timely manner to requests for scientific information as requested from customers.
• Communicate and disseminate scientific information across the internal and external stakeholder groups.
• Deliver internal and external product and disease state training as required
• Monitor and maintain up to date knowledge on all products and companies’ activities relevant to the disease area.
• Become an expert and advise where needed on the access route for products.
• Offer medical and scientific expertise to support the execution of local and global company-sponsored clinical trials, investigator-initiated studies (IIS), and non-interventional studies.
● KOL Management
• Approximately 70% of your time will be customer-facing, conducting trusted, unbiased scientific exchange in the field with prioritized stakeholders, including KOLs, Payors and advocacy organizations in support of Medical Affairs' strategies.
• Contribute KOL and customer insights related to research and medical affairs' Interests.
• Collaborate closely with the Clinical Operations to support study initiation, monitor recruitment progress from a scientific perspective, and facilitate communication with Key Opinion Leaders (KOLs) and investigators regarding scientific/medical aspects of the research.
• Obtain, assimilate, organize and report appropriate competitive and clinical intelligence in a concise, clear manner and compliant with any applicable Recordati policies and procedures.
• Develop and execute Field Medical Affairs plans at the assigned territory level in full alignment to the Medical Affairs strategies and tactics.
● Compliance Management
• Respect and abide by, all relevant Codes of Practice as they apply in Korea
• Ensure that all elements of the strategic, tactical and operational plans comply with the Codes of Practice.
• Ensure the necessary local medical and legal approval of all relevant product materials and/or events are in place prior to commercial implementation.
• Quickly and transparently communicate to the company and partner should any digressions from the above occur.
● Cross-functional Collaboration & Execution
• Achieve results for any assigned projects teams and tasks.
• Develop trust and maintain integrity with internal and external stakeholders within the global Medical Affairs and commercial organizations.
• Communicate with all medical, research and development and commercial counterparts to enhance the successful implementation of assigned or expected field medical strategies and tactics.
• Ensure the execution of activities which lead to the attainment of individual objectives and results.
● Pharmacovigilance/Medical information
• RD Korea Medical Science Liaison (MSL) may be assigned as LPVS (Local PV specialist)
• Manages any medical queries related to relevant products with the support of global MI team.
• Serve as the Medical Affairs reviewer within the LMR process for all promotional and non-promotional materials (e.g., slide decks, brochures, digital content, press releases)
Requirements
● Technical / Professional Expertise
• Active pharmacist license in Korea required
• Advanced terminal degree (MD, PhD, PharmD, DNP) strongly preferred
• Preferred over 3 years field medical experience
• Previous experience in and knowledge of rare disease or specialty care is required
• In-depth knowledge in regulatory & supply processes in Korea.
• Experience of pre-launch and launch management, including leading cross-functional teams
• Demonstrates clear ability to prioritize multiple assignments, deliver activities and results while meeting deadlines in a fast-paced working environment
• Demonstrable experience of patient journey, tracking, planning, and budgeting
• Excellent interpersonal communication and relationship building skills
• The ability to work independently and as a part of diverse teams and able to work flexibly and change priorities in line with business requirements
• Travel > 70% including field work
● Personal Specification
• Specialization in Haematology or Endocrinology will be advantageous
• Excellent verbal and written communication skills
• Fluent in English. Additional languages would be an advantage but are not essential
Information
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2차 면접전형
한글이력서, 영문이력서, 한글자기소개서 (각종 증빙서류는 서류전형합격자에 한해 추후제출)
The Others
면접은 서류전형 합격자에 개별통지 합니다.
국가보훈대상자와 신체장애자는 관련서류 제출시 관계법에 따라 우대함.
모든 서류는 반드시 MS Word로 작성하기 바랍니다.
제출하신 서류는 일체 반환하지 않습니다.
입사지원서 내용에 허위사실이 판명될 경우 입사가 취소될 수 있습니다.
기타 문의사항은 E-mail로 문의바랍니다.
Company
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레코르다티는 1926년에 설립돼 100년의 역사를 가진 이탈리아계 제약사로 이탈리아 밀라노에 본사를 두고 있고, 약 4500명 이상의 임직원을 포함, 전 세계 150여개국에 진출해 있습니다. 다발성 캐슬만병, 고위험성 소아신경모세포종 등 희귀질환(Rare Diseases) 치료제를 제공하고 있습니다.
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Recordati has been at the forefront of life-enhancing and life-changing medicines for 100 years.
With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical force, listed on the Italian stock exchange, with over 4,300 employees.
We are a group of like-minded, passionate individuals who go to extraordinary lengths for our partners, customers, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries.
At Recordati, our mantra is simple. We’ve always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Whether that is for common diseases or the rarest – we want to give people the opportunity to be the best version of themselves.
This drive will never stop. Together, we will always be reimagining tomorrow – with new ideas, new technologies and new innovations to fight diseases.
Recordati. Unlocking the full potential of life.
- 의학·과학 정보 제공 및 교류
- KOL 및 외부 이해관계자 관리
- 임상시험 및 연구 지원
- 필드 메디컬 어페어즈 계획 수립 및 실행
- 컴플라이언스 및 승인 절차 관리
- 약물감시 및 의학정보 대응
- 홍보·비홍보 자료 의학 검토
- ✓한국 약사 면허 보유
- ✓희귀질환 또는 특수질환 분야 경력
- ✓한국 내 규제 및 공급 프로세스 이해
- ✓3년 이상 필드 메디컬 경력
- ✓영어 구사 능력
- ✓70% 이상 출장 및 현장 업무 가능
- ★MD, PhD, PharmD, DNP 등 고급 학위
- ★혈액학 또는 내분비학 전공
- ★프리런치 및 런치 관리 경험
- ★교차 기능 팀 리딩 경험
- ★환자 여정 추적·계획·예산 수립 경험
- ★추가 언어 능력
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본 정보는 피플앤잡의 동의 및 허락 없이는 재배포 할 수 없습니다.



