ID: 2521
Date of Posting: Jul 20, 2026
Business Area: Medical
Job Type: Direct Employee
On site / Remote / Hybrid: On Site
Hub Office:
Seoul, KR
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Territory:
Full-Time or Part-Time: Full Time
Seniority: Associate
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At Recordati, we are united by a clear purpose: unlocking the full potential of life. With a century of history behind us, we are building the next chapter of our journey, continuing to grow while keeping patients at the centre of all we do.
What drives us is a shared belief that health, and the opportunity to live life to the full, should be within reach for everyone. This brings energy to our work, shaping how we support each other and show up every day. Our values – Better Together, Never Settle and Always Deliver – reflect this mindset, helping us to keep improving and make a meaningful difference.
Above all, these values bring to life our promise to everyone at Recordati, you can unlock your full potential. We know that people thrive when they can be themselves, are trusted and supported, and are given the opportunity to grow and make a meaningful contribution.
Are you ready to unlock your full potential?
Job 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.
Key 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)
Required Education
Active pharmacist license in Korea required
Advanced terminal degree (MD, PhD, PharmD, DNP) strongly preferred
Required Skills and Experience
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
Technical Competencies
Specialization in Haematology or Endocrinology will be advantageous
Required Behaviours and Competencies
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
Excellent verbal and written communication skills
Required Languages
Fluent in English. Additional languages would be an advantage but are not essential
Travel required in %
Travel > 70% including field work
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At Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential.
We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief.
If you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today.
