Level

GSK

Pipeline MSL(東日本)

AI in this role

Field-based Hepatology Medical Science Liaison supporting clinical development activities and scientific exchange with investigators in Japan.

medical-science-liaisonclinical-trialshepatologyscientific-communicationregulatory-compliance

Role Summary

The Hepatology Medical Science Liaison (MSL) is a field-based, non-promotional role supporting GSK’s clinical development activities in hepatology in Japan. This position is focused on supporting ongoing and planned clinical trials through high-quality scientific exchange with investigators and trial sites, contributing to the appropriate conduct of clinical research and the generation of scientific evidence.

The MSL serves as a scientific and clinical resource to investigators and internal stakeholders by facilitating trial-related discussions, identifying barriers to trial execution, and providing insights to Medical Affairs and Clinical Development teams in alignment with GSK policies and Japanese regulatory requirements.

Key Responsibilities (Japan – Pipeline Role)

•            Support GSK hepatology clinical trials by engaging with investigators, sub-investigators, and trial site staff to facilitate scientific understanding of study protocols, disease biology, and trial-related data

•            Provide scientific support for clinical trial initiation, conduct, and feasibility, including investigator meetings and trial-related educational activities

•            Identify and communicate trial-related insights, operational challenges, and scientific feedback from investigators to Medical Affairs and Clinical Development teams

•            Collaborate closely with Clinical Operations, Medical Affairs, and other internal stakeholders to support effective trial execution in Japan

•            Maintain up-to-date scientific knowledge in assigned hepatology disease areas relevant to GSK’s clinical development portfolio

•            Ensure all activities are conducted in strict compliance with Japanese regulations, GSK policies, and applicable SOPs

※職務内容および勤務地の変更範囲は会社の定めるところとする。

Basic Qualification

  • Advanced degree in a life science, medical science, pharmacy, nursing sciences, or healthcare-related discipline (e.g., MSc, MS, MPH, RN, or equivalent scientific training)

  • Clinical research, pharmaceutical industry roles, CRO, or medical affairs functions

  • Experience supporting or working with clinical trials, including interaction with investigators or trial sites

  • Strong scientific communication skills and ability to engage in evidence-based discussions with clinical experts

  • Understanding of Japanese clinical research regulations and compliance requirements (the relevant laws and regulations in the pharmaceutical industry), or demonstrated ability to rapidly acquire this knowledge

  • Language

  • Japanese: Fluent

  • English: Enough skills to understand the medical articles.

Preferred Qualification

  • Medical professional qualifications: Pharmacist, Ph.D., MD, Nurse, Veterinarian, etc.

  • Prior experience in a Medical Science Liaison, Clinical Research Associate, Clinical Scientist, or similar clinical development role

  • Experience supporting hepatology clinical trials in Japan

  • More than 3 years experience of hepatology MSL is preferable


Skills

Digital Fluency, Enterprise Thinking, External Stakeholder Management, High Impact Communication, Patient Impact

 

 

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

 

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

 

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact APACRecruitment.Adjustments@gsk.com. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

How we rate this

Pipeline MSL(東日本) at GSK rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.

Prepare for this job

A free preview built only from this posting: what it asks for, what you could be asked in an interview, and how to adjust your resume.

Skills and AI tools this role asks for

Medical Science LiaisonClinical TrialsHepatologyScientific CommunicationRegulatory Compliance

Questions you could be asked

  1. Tell me about a project where medical science liaison was part of your work. What did you do?
  2. Tell me about a project where clinical trials was part of your work. What did you do?
  3. Tell me about a project where hepatology was part of your work. What did you do?
  4. Tell me about a project where scientific communication was part of your work. What did you do?
  5. Tell me about a project where regulatory compliance was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Medical Science Liaison, Clinical Trials, Hepatology, Scientific Communication, and Regulatory Compliance. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them — a tool named with nothing behind it rarely survives a human read.

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