[Hiring] Medical Research Liaison @Amplity Health

Role Description

We are seeking a highly skilled and motivated Medical Research Liaison (MRL) to join our Medical Affairs team in Japan, focusing on Sjogren’s Syndrome. This role emphasizes expertise in clinical trial operations rather than traditional MSL experience. The successful candidate will collaborate with clinical teams, healthcare professionals, and other stakeholders to support clinical trial execution and provide scientific insights that advance understanding in the therapeutic area.

Key Accountabilities

• Clinical Trial Support:
  • Act as a key liaison between clinical trial sites, investigators, and internal clinical teams to facilitate efficient trial execution.
  • Assist in site identification, patient recruitment, and patient referral activities to support ongoing clinical trials.
  • Provide education to referral networks to enhance trial recruitment and improve service delivery.
  • Support investigators by addressing queries related to trial protocols, drug mechanisms, and clinical data.
• Scientific Expertise:
  • Stay current with the latest research and clinical data on Sjogren’s Syndrome and related therapeutic areas.
  • Communicate complex scientific and clinical information effectively to healthcare professionals, investigators, and other stakeholders.
  • Explain the rationale of the drug/molecule and its mechanism of action in a clear, credible, and engaging manner.
• Cross-Functional Collaboration:
  • Collaborate with internal teams, including Clinical Operations, Clinical Development, and Medical Affairs, to ensure alignment and consistency in clinical trial activities.
  • Gather and report insights from investigators and healthcare professionals to inform clinical and medical strategies.
  • Provide scientific training to internal and external stakeholders as needed.
• Compliance:
  • Adhere to all laws, regulations, and company policies.
  • Complete mandatory training within assigned timelines and operate with the highest ethical standards.

Qualifications

• Strong background in clinical trial operations, such as experience as a CRA, Lead CRA, Senior CRA, Project Manager in Clinical Operations, or similar roles.
• Proven ability to communicate complex scientific and clinical information effectively and credibly.
• Ideally, a strong history in clinical trials within general rheumatology (e.g., lupus, rheumatoid arthritis, or other rheumatic diseases) or general immunology.
• Advanced degree preferred (PhD, PharmD, MD, MSc), or relevant scientific discipline combined with substantial clinical trial experience.
• Business fluency in both Japanese and English is required.
• Ability to work independently and collaboratively in a dynamic, fast-paced environment.
• Willingness to travel within Japan up to 50-70% of the time.

Preferred Qualifications

• Experience in the biotech industry.
• Familiarity with Sjogren’s Syndrome or other autoimmune diseases is a strong plus.
• Strong organizational and analytical skills to manage complex clinical trial activities.