Compliance Manager / コンプライアンスマネジャー(GCP監査)

Parexel International Corporation

Tokyo, Tokyo, Japa


臨床試験が、GCP、薬事法、治験実施計画書や標準業務手順等を遵守して行われているかを評価、検証する為に、海外も含めて社内外の監査を計画、実行をマネジメントします。グローバルメンバーと協業し、クライアントと良好な関係を築き、臨床試験の信頼性向上の為に、プロセスの提案等監査をリードしていただきます。

・監査の計画、実行、評価

・監査のフォローアップ

・海外も含めた社内外へのアドバイス、サポート

・クライアントによる監査、規制当局による査察のサポート

・社内コンプライアンス向上のサポート

・QAツール、QAシステムのアップデート

Job Purpose: Have a high level of knowledge and experience of appropriate GxP compliance and other applicable regulations and laws, Parexel procedures and appropriate Parexel processes to conduct audits and provide expert advice to internal and external clients. To effectively lead, matrix manages, develop, and implement assigned projects. To exhibit a high degree of flexibility and initiative, demonstrate the ability to follow up on multiple tasks and projects, and possess the ability to handle confidential information diplomatically.

Specialized Area:

The Compliance Manager will have a primary role in the management/coordination/oversight of QA compliance GxP activities in a specific geographical and/or functional/specialist area, as assigned by QA Senior Management. Alternatively, or in addition, the Compliance Manager can act as the QA Lead / QA Lead back-up for a Strategic Partnership or a client account for which QA representation is needed. Other duties may include the Auditor Coordinator role, as assigned.

Key Accountabilities:

• Work independently and as part of the QA team

• Act as expert GxP consultant in relevant area to groups within the Parexel organization and sponsors

• Train new and existing QA personnel

• Train and educate operational staff by the development and presentation of training courses

• In liaison with the QA management, promote compliance within the company and represent QA, as required

• Build, develop, and maintain good working relationships with internal and external customer

• groups

• For area of specialization, work with internal customers and develop and execute strategic audit

• Deputize for QA management within area of specialization

• Review the work of the matrix team to ensure consistency and quality within the group

• Act as a contact with members of Regulatory Authorities and / or sponsors; help lead in their

• audits / inspections in agreement with QA management

• Contribute to the information provided to QA management to summarize quality issues arising

• from audits and other related activities, as requested

• Plan and conduct complex audits / mock office inspections in agreement with QA management

• Ability to review and, if necessary, identify improvements that enhance the quality and clarity of

• audit reports

• Assist QA management in the development and implementation of strategic procedures and

• working practices to ensure continuous quality improvement

• Maintain relevant knowledge of both local and international auditing and appropriate GxP

• requirements and developments as they impact Parexel international SOPs and compliance

• with GxP, and communicate these to the QA team and QA management, as applicable

• Be familiar with GxP required computer system validation requirements

• Maintain and / or develop records / documents for assigned areas

• May serve as a member of industry association boards, task forces, and committees and / or as

• chairperson or officer of one or more professional associations. Contributes expertise to

• professional societies, academic, or other similar groups influential in his / her area of expertise

• Develop and maintain network contacts with other quality assurance professionals

• Travel on assignment

• Other duties as assigned

QualificationsPMDA等、規制当局の査察対応の経験

GCP監査、ベンダー監査、治験実施医療機関監査対応等監査の実務経験必須

ビジネスレベル英語力

Minimum Work Experience

Extensive experience in quality assurance, regulatory affairs, auditing, or other relevant area including applicable GCP auditing


2021-05-18 00:05:35


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