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Ophthalmology Medical Liaison

2 months ago

Hong Kong, Central and Western District, Hong Kong SAR China Santen Inc Full time

[HONG KONG] Medical Science Liaison

Full-time

Company Overview

Santen is a dedicated life sciences organization with a rich 130-year legacy, exclusively focused on ophthalmology. As a globally recognized entity originating from Japan, we operate in over 60 countries, committed to providing innovative solutions and treatments for eye health while addressing vision-related societal challenges worldwide.

ROLE OBJECTIVE

The Medical Science Liaison (MSL) for HONG KONG is pivotal in fostering and sustaining professional relationships with key opinion leaders (KOLs), healthcare practitioners, and other essential stakeholders within the medical field. This role's primary focus is to deliver scientific and medical knowledge regarding designated therapeutic areas or products, thereby enhancing comprehension, education, and acceptance of the company's medical offerings and research. The MSL acts as a conduit between Santen and the medical community, aiding in the formulation and implementation of medical affairs strategies. A robust scientific foundation, exceptional communication abilities, and the capacity to interpret and relay intricate medical information are essential for this position.

Key Responsibilities

KOL Engagement and Relationship Management

Identify, cultivate, and sustain effective relationships with KOLs, healthcare professionals, and academic institutions relevant to the assigned therapeutic domain. Collaborate with KOLs to collect insights, feedback, and medical/scientific data to inform the company's medical affairs and commercial strategies as well as research initiatives. Capable of implementing and overseeing Early Access Programs or Compassionate Use Programs, with a strong emphasis on patient-centric approaches.

Scientific Communication and Education

Distribute pertinent and current scientific and medical information to healthcare professionals, KOLs, and internal stakeholders, ensuring precise and compliant communication. Address medical inquiries (including unsolicited off-label questions) from healthcare professionals and KOLs, supplying evidence-based and scientifically sound information regarding products, clinical data, and disease management. Organize and present scientific presentations and educational initiatives for healthcare professionals and internal teams, keeping them updated on the latest advancements in the therapeutic area.

Clinical Research Support

Partner with clinical development teams to provide medical insights on study protocols, study design, and data analysis plans to ensure alignment with global or regional strategies and objectives. Assist in identifying and recruiting investigators for clinical trials and observational studies. Facilitate the communication of study outcomes to internal and external stakeholders and aid in interpreting the clinical significance of data.

Cross-functional Collaboration

Contribute to the development and execution of medical affairs plans, including medical publications and medical information strategies. Collaborate closely with cross-functional teams, including marketing, sales, and regulatory affairs, to provide medical insights and support product launch and lifecycle management activities. Participate in medical and scientific conferences, symposia, and congresses to remain informed about the latest scientific advancements and represent the company's interests.

Compliance and Regulatory

Ensure all activities and interactions comply with industry regulations, company policies, and compliance guidelines. Maintain a comprehensive understanding of relevant laws, regulations, and codes of conduct governing medical affairs activities.

Qualifications

Advanced degree in a relevant life sciences discipline (e.g., MD, PharmD, MPH, PhD). Over two years of experience in the pharmaceutical/biotech sector, clinical practice, or academia, preferably within ophthalmology. Strong scientific aptitude and the ability to comprehend and interpret complex clinical data. Excellent communication and presentation skills, with the capability to effectively convey scientific information to diverse audiences. Proven track record of building and maintaining relationships with KOLs and healthcare professionals. Familiarity with regulatory guidelines and compliance requirements in the pharmaceutical industry. Demonstrated ability to work collaboratively in a cross-functional team environment. Strong organizational and time-management skills to effectively manage multiple projects and priorities. Proficient in English, both spoken and written. Willingness to travel based on business requirements.

Additional Information

Develop your career at Santen

A career at Santen presents an opportunity to make a meaningful impact. Through our long-term vision outlined in Santen 2030, we are dedicated to being a Social Innovator - addressing the social and economic needs of individuals with visual impairments. Our team members worldwide leverage their diverse talents to unlock new modalities and drive innovations for patient outcomes, education, and treatment. At Santen, we believe in empowering all our team members with flexible working arrangements and a highly inclusive work environment.

The Santen Group is an Equal Opportunity Employer. We are committed to building diverse teams and ensuring a safe and inclusive physical and virtual workplace for every one of our team members. All employment decisions are based on business needs, role requirements, and individual qualifications, regardless of race, color, ethnicity, national origin/ancestry, religion, sexual orientation, gender, gender identity/expression, age, disability, medical condition, marital status, veteran status, or any other characteristic protected by law.

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