Sso Associate Clinical Project Manager

Job description

臨床試験の現場を動かし、患者さんに届く医療のスピードと質を支える——このポジションは、その最前線で活躍できる役割です。SSO Associate Clinical Project Managerとして、あなたは担当国における臨床試験の計画から実行、クローズアウトまでをリードし、多様なステークホルダーと連携しながら、確実で高品質な試験運営を実現します。日々のオペレーションを通じて専門性を高め、グローバルチームの一員として成長しながら、革新的な医薬品を患者さんに届ける確かなインパクトを生み出せるポジションです。Play a pivotal role at the heart of clinical trial delivery, where your work directly supports the timely and high‑quality development of innovative medicines for patients.

As an SSO Associate Clinical Project Manager, you will lead country‑level execution of clinical studies from initiation through close‑out, working closely with cross‑functional and global teams. This role offers a unique opportunity to build strong project management expertise, collaborate in a global matrix environment, and make a tangible impact on how clinical trials are delivered every day.

Responsibilities

Key Responsibilities担当国における臨床試験の計画から実行、クローズアウトまでを一貫してリードするLead end‑to‑end execution of assigned clinical studies at the country levelグローバルおよび国内の関係者と連携し、試験の進捗・課題・リスクを適切に管理するCollaborate with global and local stakeholders to manage study progress, risks, and issues試験スケジュール、進捗、KPIを管理し、品質と納期の両立を確保するManage timelines, progress, and key performance indicators to ensure quality and delivery施設およびClinical Research Associateと連携し、被験者組み入れ目標の達成を推進するDrive patient recruitment performance in collaboration with sites and Clinical Research Associatesデータ品質および規制遵守を確保し、GCPおよび社内基準に沿った試験運営を行うEnsure data quality and regulatory compliance aligned with

Good Clinical Practice and internal standardsモニタリング結果をレビューし、課題の是正およびエスカレーションを適切に実施するReview monitoring outputs and drive timely issue resolution and escalation監査・査察対応および継続的改善活動を通じて、試験運営の質向上に貢献するSupport audit readiness and continuous improvement initiatives to enhance trial executionEssential Requirements科学系またはヘルスサイエンス分野の学士号を有していることBachelor’s degree in a scientific or health‑related discipline臨床試験における実務経験を3年以上有し、モニタリングまたは試験管理に携わった経験があることAt least three years of experience in clinical research, including trial oversight or monitoring臨床医薬品開発プロセス全般への理解を有し、試験運営に関する知識を備えていることSolid understanding of the clinical drug development process and study executionグローバルかつマトリクス型の環境で協働できる能力Ability to work effectively in a global matrix environment国際的な臨床試験基準および規制要件への理解Knowledge of international clinical trial standards and regulatory requirements英語での円滑なコミュニケーション能力（読み書き・会話）Fluency in written and spoken

EnglishDesirable Requirements臨床試験におけるプロジェクトマネジメントまたはStudy Lead経験Experience in clinical trial project management or study leadership多国間試験やグローバルチームとの協働経験Experience working with global or multinational study teamsBenefits and RewardsRead our handbook to learn about all the ways we’ll help you thrive personally and professionally:https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdfCommitment to Diversity and InclusionNovartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.Accessibility and AccommodationNovartis is committed to working with and providing reasonable accommodation to individuals with disabilities.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Additional InformationBe aware of fake job advertisements and job offers.

Novartis does not make job offers without interviews and never asks candidates for money. All our current job openings are displayed here. If you have encountered a job posting or been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond, send money, or provide personal information.

Join our Novartis Network

Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network