Job Description

We are seeking a dedicated and experienced Sr CRA and this role is perfect for someone with a keen interest in developing their skills in clinical monitoring.

職務内容

* Managing and providing oversight to the progress of clinical studies.
* Ensuring that clinical trials are conducted in accordance with regulatory and ethical guidelines.
* Overseeing data management and ensuring the accuracy of collected data.
* Developing and maintaining relationships with investigative sites.
* Assisting in the development of study documents and trial plans.
* Providing training to site staff and monitors.
* Participating in the preparation and review of study reports and clinical documents.
* Coordinating with other departments to ensure the smooth running of clinical trials.

理想の人材

A successful Sr CRA should have:

* An educational background in Life Science or a related field.
* Proven experience in managing clinical monitoring.

条件・待遇

* The flexibility of a HYBRID work arrangement.
* A generous package.

We believe that our employees are our most valuable asset, and we are committed to providing a supportive and inclusive work environment. If you are a dedicated Sr CRA looking to make a difference in the Healthcare industry, we encourage you to apply.

Page Group Japan is acting as an Employment Agency in relation to this vacancy. - Experienced CRA
- Fluent Japanese

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