Experienced Clinical Research Monitor

Tokyo 23 Wards 外資系企業 ¥5,000,000 - ¥9,000,000 per year Foreign Multinational Work from Home or Hybrid View Job Description
At the front line of communication with stakeholders at hospital sites / clinics, you'll manage clinical aspects of full-service global trial projects. Your responsibilities will include ensuring timelines, targets, and standards are met for clinical research projects spanning various therapeutic indications. You will be responsible for upholding subjects' rights, safety, and well-being, as well as ensuring compliance with data quality standards.
  • CROの世界的なリーディングカンパニーであなたのキャリアをスタートさせませんか。
  • 画期的な医薬品・医療機器の開発を支援するグローバル・リーダーの一員になる

About Our Client



  • Internationally renowned CRO with 30 years of experience in providing expert delivery of pivotal Phase 2 & 3 Oncology, Hematology, Rare Disease, Immunology, Infectious Disease studies expansion worldwide. Currently expanding business within Japan and APAC region.

Job Description

  1. Manage the clinical aspects of full-service global trial projects.
  2. Communicate effectively with stakeholders at hospital sites and clinics, serving as the front line contact.
  3. Ensure adherence to timelines, targets, and standards for clinical research projects in various therapeutic areas.
  4. Prioritize subjects' rights, safety, and well-being throughout the trial process.
  5. Maintain compliance with data quality standards.
  6. Collaborate with multidisciplinary teams to achieve project objectives.
  7. Monitor and assess project progress, identifying and addressing any challenges or deviations.
  8. Provide support and guidance to site staff regarding clinical trial procedures and requirements.
  9. Contribute to the development and improvement of clinical trial protocols and processes.
  10. Stay informed about regulatory requirements and industry best practices related to clinical research.
  11. Document and report trial activities and findings accurately and comprehensively.

The Successful Applicant

  • Experience of at least one year as a CRA.
  • Additional experience as a CRC, MR, or co-medical is welcomed.
  • English proficiency with a TOEIC score of 500 or higher is desirable.
  • Native level Japanese is mandatory
  • Bachelor's degree or above, preferably in a science-related field such as pharmacy or natural sciences from a four-year university.

What's on Offer



Great opportunity to contribute to the establishment of a new CRO in JapanCRA Perks

    • Competitive Travel bonus (Variable Compensation Plan)
    • Annual Company Bonus
    • Retention Bonus
    • DC Pension Plan
    • Life Insurance
    • Annual Merit Increase
    • Opportunity for leadership positions/career advancement
    • Opportunity to work from home
    • Cell phone and laptop provided
    • Secure your own desk
    • Flexible work hours across days within a week
    • Office furniture allowance
    • Dedicated CRA Training and Development
    • Vacation time, paid company holidays (plus floating holidays), sick time
    • Casual Dress Code

Potential career path as a CRA

  • Clinical Operations Line Management
  • Clinical Project Management
  • Pharmacovigilance / Drug Safety
  • QA Auditing
  • SMO Management
  • Site Management / Contracting
  • Regulatory affairs
  • MSL / Medical Science Liaison
  • Medical writing
  • Clinical Data Management / Biometrics



Contact
Ed Marsden
Quote job ref
JN-052024-6418094
Phone number
+813 6832 8981

Job summary

Function
Life Sciences
Specialisation
Clinical Operations
What is your area of specialisation?
Healthcare / Pharmaceutical
Location
Tokyo 23 Wards
Job Type
Permanent
Consultant name
Ed Marsden
Consultant phone
+813 6832 8981
Job Reference
JN-052024-6418094
Company Type
Foreign Multinational
Work from Home
Work from Home or Hybrid

Diversity & Inclusion at Michael Page

We don't just accept difference - we celebrate it. We encourage applicants from all backgrounds to apply for this role and are committed to building inclusive, diverse workplaces where everyone can thrive. If you require any support or reasonable adjustments during the recruitment process, please let us know.