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Updated 2024-05-08
Activated 2024-05-08
Activated 2024-05-08
Experienced Clinical Research Monitor
- Recruiter
- Staff Level
| This posting is managed by: | Michael Page International Japan K.K./マイケル・ペイジ・インターナショナル・ジャパン株式会社 |
|---|---|
| Company Name | Global CRO |
| Job Type |
 Health/Nursing - Nurse Medical/Pharmaceutical/Bio/Fabric/Food - Pharmacist |
| Industry | Pharmaceuticals |
| Location |
Asia
Japan
Tokyo
|
| 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. 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 Japan CRA 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 Page Group Japan is acting as an Employment Agency in relation to this vacancy. |
| Company Info |
* 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. |
| Working Hours |
Flex time available Core hours: 11:00 - 15:00 |
| English Level | Business Conversation Level (TOEIC 735-860) |
| Japanese Level | Fluent(JLPT Level 1 or N1) |
| Salary | JPY - Japanese Yen JPY 5000K - JPY 9000K |
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Recruiter
Michael Page International Japan K.K./マイケル・ペイジ・インターナショナル・ジャパン株式会社
