Clinical Project Manager

Make your mark for patients

患者さんのためにあなたの力を発揮してください

フルリモート不可/Hybrid work model

Please check if the candidate has applied for a job at UCB in the past year.一年以内のご応募歴を必ずご確認ください

Please make English and Japanese resume combined in one document to submit英語と日本語の書類を一つに纏めてご提出ください

If you have any questions please contact recruiting team 質問がございましたら採用チームまでお問い合わせください

JOB SUMMARY
Primary Purpose / Regulatory Responsibilities:
Accountable for the delivery of patient-centric studies from protocol design through to study report and archiving. These can be all types of study from First in Human to Phase 4 across all geographies and in all UCB theraputic areas including Gene Therapy.
Accountable for the effective interface and influential stakeholder management between UCB Phase 1 Units Clinical Research Organizations (CROs) and other vendors to ensure assigned studies are delivered according to contract specifications with high quality meeting all major milestones and to budget.
Lead study specific decision making and develop strategies for increasing study efficiencies.

MAJOR RESPONSIBILITIES
Accountable for the leadership and delivery of all assigned UCB sponsored clinical trials through effective internal and external team stakeholder management in a matrix organisation.
Responsible for operational updates issue/mitgations ensuring open transparent communication with team members line management and Clinical Strategic Partnering escalating within and outside the team as needed.
Demonstrate robust oversight of sponsor-delegated activities by regularly reviewing CRO/Phase 1 Unit performance including TMF status through use of KPIs metrics and deliverables (such as SQV Impact) with a focus on trial subject safety data quality and critical activities that might delay the project or impact budget.
Responsible for Site Engagement strategies to support study recruitment at sites. Become familiar with the competitive landscapes; engage with Key Opinion Leaders (KOLs) investigational sites patient advocacy groups and other relevant organizations.

For assigned studies be the key internal clinical operations contact working closely with the respective PDL and other team members.
During start-up articulate study scope goals and expectations of UCB to the CRO/Phase 1 Unit and ensure all relevant information that may impact the set-up of the trial is highlighted and accounted for in the study planning.
Responsible for detailed planning of study timelines to enable timely access and prompt decision making for all data for Safety Monitoring/Data Monitoring Committees planned Interim Analyses final data reporting for Results Interpretation Meetings and final Clinical Study Report (CSR).
Responsible to manage track and ensure accuracy of study budgets in UCB systems including the forecast and accrual information.
Work with CRO partners to define a study specific monitoring strategy. Review Monitoring Plans and CRA generated reports (as appropriate).
Support any audit/inspection activities including audit/inspection readiness ensuring findings are appropriately addressed in a timely manner and overall compliance with regulations (eg ICH GCP) and applicable quality standards at all times.
Identify issues/gaps in processes and interfaces with other groups and departments and develop recommendations for resolution. Contribute to process improvement initiatives and share best practice experiences with line manager peers and Partner CROs.

EDUCATION & QUALIFICATION
Education necessary for this role (not the education of the person)
Education Level :Bachelors Degree

COMPETENCIES
Include specific skills behaviors and knowledge necessary to meet the objectives of the role
Technical:
- Operational clinical project management experience (P1-4) including an understanding of the complexities of Global Clinical Development and Operations.
- Ability and experience to manage study feasibility assessments vendor management study start-up process different modalities of outsourcing data management risk-based quality management.
- Solid understanding of budgeting process budget follow-up and forecasting.
- Proficiency in the Microsoft office suite.

Leadership:
- Ability to lead and maintain high performing multi-disciplinary teams in a matrix environment.
- A flexible proactive and adaptive management style.
- Excellent time management and organizational skills.
- Results and problem solving oriented. Presents can do attitude.
- Effectively manage and influence all stakeholder relationships.
- Excellent communication skills demonstrating clear and articulate verbal written and presentation skills with excellent command of the English language.
- Ability to manage conflict and achieve consensus in a team.

患者さんのために価値を創造しご自身の力を発揮する準備ができているとお感じでしたらぜひ私たちにご連絡ください

会社概要

UCBは神経および免疫領域に注力するグローバルなバイオ医薬品企業です世界中で約8500人の社員が患者さんからインスピレーションを受け科学の力で前進しています

UCBで働く魅力

UCBでは単に業務をこなすのではなく価値を創造することを大切にしています私たちは挑戦を恐れず協力し合い革新を追求しながら患者さんのために成果を出すことを目指しています
誰もが尊重され受け入れられ最善を尽くせる平等な機会がある思いやりと支援に満ちた文化が根付いています
私たちは常にその先を目指し患者さん社員そして地球に対して人間らしさを大切にした価値を提供しています
UCBで働くことで自分自身の成長を実感し自由にキャリアを築き可能性を最大限に引き出すことができます

UCBでは機会均等を重視していますすべての採用決定は法律で保護されているいかなる属性にも関係なく行われます

選考プロセスにおいてご自身の強みや能力を十分に発揮できるよう配慮が必要な場合は以下のメールアドレスまでご連絡ください

なおこの問い合わせ先では選考における特別な配慮に関するご相談以外はお受けできませんのでご注意ください