Experienced Clinical Research Monitor

東京23区 外資系企業 年収 500万円 - 900万円 外資系企業 在宅可・ハイブリッド勤務可 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

企業情報



  • 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.

職務内容

  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.

理想の人材

  • 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.

条件・待遇



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



コンタクト
Ed Marsden
求人番号
JN-052024-6418094
電話
+813 6832 8981

求人情報

分野
ライフサイエンス
職種
治験
業界
ヘルスケア・製薬
勤務地
東京23区
雇用形態
正社員
担当コンサルタント
Ed Marsden
担当コンサルタントの電話番号
+813 6832 8981
求人番号
JN-052024-6418094
企業タイプ
外資系企業
勤務形態
在宅可・ハイブリッド勤務可

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