Location: Japan - Tokyo
Salary: 8000000 - 13000000 JPY
Job Function: Clinical Development
Reference: JO-171102-139682
Industry: Life Sciences & Healthcare
Sub-Industry: Pharmaceuticals

Purposes of the job are,

  • To facilitate/support planning and execution of sponsored clinical studies, ensuring alignment of affiliate Development TA and Development Operations
  • To generate documents with high medical/scientific quality relevant to clinical studies and reporting to health authority

Key activities include,

Clinical Development

  • Ensure alignment of affiliate development strategy, study design and execution between Affiliate Development TA and Affiliate Development Operations/external partners
  • Contribute to the design of the protocol, engaging external experts
  • Communicate relevant local medical environment
  • Assist DFM in identifying qualified investigators/study sites
  • Support Clinical Development Operations activities.
  • Support CRA in conducting Site Engagement and Site Evaluation visits, and support remote site evaluation and central monitoring set up.
  • Develop and execute study-specific Site Relationship Management Plan for investigators to improve company and investigator relationship, including the below activities as required:
    • Scientific interaction visit
    • IRB support visit
    • Relationship issue management visit (Apology visit)
    • Enrollment support visit
    • Act as an interface between study team and Project Team
  • Coordinate providing scientific/medical content to address IRB/EC/national authority issues.
  • Assist Affiliate Development Operations in protocol interpretation
  • Scientifically review and edit documents relevant to global development and local clinical activities
  • Review translated version of documents relevant to global development and local clinical activities
  • Author/review/edit assigned part of CTD collaborating with Medical Director/Sr. Medical Advisor and Medical Writer
  • Support Affiliate Medical Directors/Sr. Medical Advisors in developing responses to queries from regulatory agencies
  • Organize advisory board meetings; data monitoring committees and steering/executive committees coordinating contracts
  • Handle Consultancy Agreements and other Service Agreements with external experts for contracts owned by affiliate Development TA

Basic Qualifications

  • BA/BS/BSc
  • Three (3) or more years of clinical research experience and/or academic research experience including experience working on clinical trials
  • Plus > 2 year experience in study site-monitoring
  • Native level Japanese
  • Language proficiency in English (business discussions, reading, and writing)