Project Leader / プロジェクトリーダー(東京/大阪/在宅)

Posted 3 Days Ago
Be an Early Applicant
2 Locations
Remote
Senior level
Pharmaceutical
The Role
As a Project Leader at Parexel, you will manage clinical development projects ensuring compliance with regulations while leading cross-functional teams and maintaining relationships with clients. You will be responsible for planning, coordinating with various departments, and overseeing project timelines, costs, and quality outcomes to guarantee client satisfaction and expected benefits.
Summary Generated by Built In

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

クライアントである製薬会社等と良好な関係を築き、さまざまな要望・期待に応え、満足していただけるサービスを提供することで、当社とクライアント双方にとってWin-Winとなるようプロジェクトをリードしていただくポジションです。

  • 契約事項、薬事法、GCP等の関連法規、SOP等を遵守し、プロジェクト全体を管理する。
  • 受託業務内容を熟知し、業務全体の計画立案、各部門との調整、クライアントとの折衝を行う。
  • 臨床開発プロジェクトのプロジェクトマネジャーとして、部門横断的にプロジェクトチームをリードし、プロジェクトチームの発足からプロジェクト終了までの全てのプロセスにおいて、タイムライン、コスト、人員を管理する。具体的には、各プロジェクトが、Qualityを担保しタイムライン通りにマイルストーンを達成できているか、各部門リーダーから報告を受け、確認する。
  • クライアントの期待に応えるため、利益や品質の成果責任を果たせるようプロジェクトをリードする。
  • クライアントとの良好な関係を維持し、クライアントの満足度を向上させ、想定された利益を確保する。
  • 電話/Teamsなどを通して、カウンターパートとの情報交換やアラインメントを図るサポートを行う。

【応募条件】

  • 医薬品のプロジェクトマネジメント経験あるいは開発業務のリーダー経験
  • ビジネスレベルの英語力
  • オンコロジー領域経験あればなお可
  • PMの資格として、米国のPMI(Project Management Institute)が認定するPMP (Project Management Professional)資格を有すれば、なお可
  • CRO勤務経験者歓迎
The Company
HQ: Durham, North Carolina
20,524 Employees
On-site Workplace

What We Do

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.

Community Guidelines
Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:

• Abusive, harassing or threatening to others.
• Defamatory, offensive, obscene, vulgar or depicting violence.
• Hateful targeting by race/ethnicity, age, color, creed, religion, gender,
sexual preference or orientation, nationality or political beliefs.
• Sexually explicit or pornographic.
• Fraudulent, deceptive, libelous, misleading or unlawful.
• Referencing criminal or illegal activity.
• Spamming.

We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

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