ジェンマブは革新的な抗体医薬の開発に注力し、患者さんの生活を改善することに力を尽くしています。

私たちは、extra[not]ordinary な未来を共に築くことを使命とし、革新的な抗体製品の開発や人々を感動させる抗体医薬品で、がんやその他の深刻な病に苦しむ患者さんの生活を根本的に変え、治療の未来を切り拓いています。

ジェンマブは思いやりがあり、率直で、患者さんに貢献したいという強い思いを持った人たちがともに働き、科学に基づく変化をもたらします。大胆さと高潔性を持って行動し、新しい未来をつくることを目指すこと が、この使命を果たすために不可欠だと信じています。

私たちは大きな志を掲げ、楽しく、そして思いやりの心を忘れずに、日々意義のある仕事に取り組んでいます。私たちは、個々のユニークな貢献を受け入れ、それらを原動力として、患者、ケアパートナー、ご家族、そして社員のニーズを満たす革新的なソリューションを生み出し、育み、維持するグローバルな企業文化の構築に努めています。

私たちの想いに共鳴し、自分らしく活躍できそうだと感じたら、ぜひ一緒に働きましょう。

Position Summary:

The position is responsible for all the safety case processing and safety data management matters regarding all products in both the development phase and the post-marketing phase. This position leads regional Safety Opes & DM function group and also may act as a deputy safety supervisor (deputy Anseki).

Primary roles & responsibilities include, but are not limited to;

Safety operation (case processing) and safety data quality management

Define/develop Safety Operations process and strategies.

Define/develop and maintain required process documents i.e. safety related QMS documents, safety monitoring plan etc.

Ensure complying with the local/global regulatory requirements and reporting due date. 

Oversight/perform real time/retrospective QC for safety case data entry and scheduled reports.

Oversight/conduct the daily cases monitoring in the safety system workflow.

Oversight SAE Reconciliation activities including review and approval of the reconciliation plan and generation of SAE reconciliation listings.

Ensure/conduct data corrections and case deletions upon request or as needed.

Work with other relevant Genmab departments to standardize the safety reporting process language in documents, safety reporting forms according to the local/global reporting requirements.

Provide guidance on questions around safety operations based on not only company conventions, but also ICH and regulatory guidance.

Introduction, implementation and maintenance for any safety related systems, any other computer systems and tools

Lead/facilitate project for safety related systems and tools.

Act as the primary business contact at Drug Safety Japan to IT team and GDS regarding requirement specification, system development/implementation plan and validation testing.

Generate required periodic listings or ad-hoc tabulations.

Collaborate with global Safety Opes & DM team regarding study start-up activities, MedDRA version up activities.

Oversee appropriate maintenance for required drug codes (J-Drug Code) or company defined code in the company safety system.

Review and/or submit configuration or customization requests for any safety related system.

+ if could, the following roles may be assigned for support to global Safety Opes & DM role.

Perform User Acceptance Test (UAT) on Safety Related Forms in EDC, ensuring correct dynamics and edit checks. Provide comments on the e-Safety Reporting Form Specifications document and perform UAT.

Oversight safety CRO activities and coordinate CRO contract/ AE reporting agreement

Ensure/lead vendor selection process and implement outsourcing activities for Safety Opes & DM related topics according to both local/global requirements.

Ensure/Oversight preferable vendor for PV operation activities including the relevant budget management.

Oversight the appropriate case intake of safety reports and case processing due date.

Oversight other activities related to safety operations including ICSR submission or distribution to Regulatory authorities/ECs/IRBs/Investigators/Business Partners.

Escalate/propose appropriately improvement/function growing plan to local head of Drug Safety and required global stakeholders.

Ensure reliability of GVP related activities for case processing and safety compliance.

Have appropriate safety communication and work in collaboration with global counterpart or DS&PV team.

Establish good relationships with global counterparts.

Closely communicate the product status/updates of safety regulations in timely manner from system configuration perspective.

Take appropriate actions to local and global DS for providing the training program on the responsible topics.

Required Technical Skills and Competencies

• Minimum 6+ years of relevant experience in Safety Operations or Safety Data Management area
• Experience executing process/projects in own area (e.g. regulations & reporting requirements, preparation of post-marketing and clinical safety assessment, safety case processing, PV data systems and PV report generation)
• Experience guiding team members around complex issues on SDM topics.
• Advanced knowledge of GCP, GVP, GPSP requirements and relevant global GxPs requirements, regulatory compliance and documentation requirements relevant for scope of work.
• Sufficient knowledge of ICH E2B(R2) and (R3) specifications and entry guidance.
• Sufficient knowledge of compliance relevant regulatory obligations, especially pharmacovigilance reporting rules and timelines.
• Experience with clinical and post-marketing case processing, including MedDRA and required drug dictionary coding and narrative writing
• Experience close collaboration with other departments in local and global including license partners.
• Must have strong English capability to communicate with global stakeholders effectively (intermediate business communication level or above)
• Bring out-of-box thinking and will to make it happen

Optional Experience & Skills:

• Experience of leading projects on safety system release/significant upgrades in globally or locally.
• Experience of people management.
• Knowledge and experiences of ARGUS safety system and/or any other Safety systems
• Knowledge of ERES (Electrical Records Electrical Signature) / e-documentation requirements
• Re-examination experiences (ICSR case processing part in the inspection, or Response to PMDA queries)
• Clinical (Study) data management experience or EDC for clinical trial data collection experience.
• Clinical operation / monitoring experience
• Experiences of activities related to Pharmaceutical Manufacturing/Marketing Company License (Gyokyoka):The Initial License Registration (製造販売業許可申請), The renewal of License (製造販売業許可更新).

場所

ジェンマブは、可能な限り柔軟な働き方を取り入れることで、社員のワークライフバランスの向上に取り組んでいます。

私たちのオフィスは、オープンな環境の中で従業員同士がつながることを目的としています。オフィスでも、リモートワークでも、お互いにつながることを大切にし、イノベーションを生み出します。

 ジェンマブについて

ジェンマブは、革新的抗体医薬を通じて患者さんの生活を向上させることを目指す、グローバルバイオテクノロジー企業です。

25年間、情熱的で革新的、そして協力的なチームが、次世代抗体技術プラットフォームを開発し、トランスレーショナルサイエンス、定量科学、データサイエンスを活用することで、独自のパイプラインを確立してきました。このパイプラインには、二重特異性T細胞エンゲージャー(bispecific T-cell engagers)、抗体薬物複合体(ADC)、次世代免疫チェックポイントモジュレーター、エフェクター機能強化抗体などが含まれています。

ジェンマブのビジョンは、2030年までに、人々を感動させる抗体医薬品でがんやその他の深刻な病に苦しむ患者さんの生活を根本的に変えることです。

ジェンマブは、1999年に設立されたデンマーク・コペンハーゲンに本社を構え、北米、ヨーロッパ、アジア太平洋地域に国際的な拠点を展開しています。

ジェンマブでは、候補者個人データ及びプライバシーを重要なものと認識しており、個人情報の保護に関する法律その他の関係法令を遵守しています。個人情報の取扱いにご同意いただいた上、ご応募ください。

詳細は、以下リンク先よりご確認ください:Job Applicant Privacy Notice )