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Embrace the opportunities for personal and professional growth


パレクセルは、臨床開発の上流から下流までのそれぞれの専門領域で、国内外の多くのお客様に高度なソリューションを提供するプロフェッショナル集団です。 パレクセルは、新しい薬や治療法を、それらを必要としている人々にいち早く届けることを目指し、日々の業務に取り組んでいます。

Clinical Research Associate/臨床開発モニター(東京・大阪・神戸・在宅可)

求人ID 53013BR ロケーション 東京都, 東京都 仕事内容


•モニタリング ・GCP(Good Clinical Practice)、治験実施計画書、SOP(Standard Operating Procedure)に則って治験が進んでいるかを確認
•直接閲覧(SDV: Source Data Verification)を実施し、症例報告書(CRF: Case Report Form)とカルテ等が一致しているかを照合し、回収
•IRB (Institutional Review Board)への文書提出及び手続き
•治験の終了手続き など


•配属部署: 臨床開発部
•配属オフィス: 東京・大阪・神戸(一部在宅可)

Your time here

At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they’re set up for success. As the clinical sites’ sole point of contact, this includes addressing and resolving site issues and questions. You’ll also manage site quality and delivery from site identification through to close-out.

As a CRA, Parexel will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, Parexel could be your next home.

What you’ll do
*Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
*Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
*Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
*Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
*Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
*Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.


CRA経験(経験年数1年以上) ※経験領域・疾患は問いません



More about you

On your first day we’ll expect you to have:

*Previous relevant work experience (preferred).
*Ability to perform clinical monitoring activities under supervision from the COL/LM.
*Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline.
*Strong interpersonal, written, and verbal communication skills within a matrixed team.
*Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
*A client-focused approach to work and flexible attitude with respect to assignments/new learning.
*The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
*An honest and ethical work approach to promote the development of life changing treatments for patients.
*Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic *Document Management System (EDMS) and MS-Office products such as Excel and Word.

A little about us

Parexel is proud to be a leading Clinical Research Organization with colleagues across the globe. As a member of our team, you’ll get to know your coworkers on a personal level. Have a question? A clinical research leader, project team member, technology “super user” or collaborator are a phone call away. Our clinical research teams meet regularly to have discussions in an open environment, allowing our team members to share their expertise and promote learning within the team. Management supports and encourages career growth through consistent performance discussions and evaluations. Whether your interest is to progress into a more senior level CRA role, into line management, Quality, Project Leadership or a variety of other positions, Parexel prides itself on career opportunities for our employees.









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