实验室项目经理I
Labs Project Manager I
职位名称：实验室项目经理 I
工作地点：远程，英国
工作地点类型：远程
工作合同类型：全职
职位级别：
工作时间安排
标准（周一至周五）环境条件
办公室职位描述
推动临床创新。实现科学卓越。
在Thermo Fisher Scientific，您将加入一家处于临床研究和实验室科学前沿的全球组织。与PPD合作，我们支持全球领先的制药和生物科技组织——在过去五年中成功交付了超过2700项临床试验，覆盖100多个国家。
我们正在寻找一名实验室项目经理，负责领导和协调临床试验项目中的中央实验室活动。这是一个高影响力职位，需要强大的运营监督、跨职能领导力和客户参与。
职位职责：项目经理是运营部门、附属机构、赞助商和实验室团队之间的主要联络人。您将负责所分配临床方案和项目的启动、维护和结题活动，同时支持更广泛的项目管理职能。
主要职责：
- 作为所分配临床试验的主要项目经理，包括复杂、多方面的研究。
- 作为内部实验室功能和外部客户的主联系人。
- 独立识别、管理和缓解研究层面的风险；根据需要升级跨职能或重大问题。
- 领导研究启动活动，包括方案和修订审查、里程碑规划、风险评估和预算监督。
- 协调实验室运营、物流、数据管理、质量、IT和外部供应商等跨职能团队，确保顺利执行。
- 管理研究时间表、交付物、相互依赖关系和绩效指标，以确保按时和高质量的数据交付。
- 保持符合SOP和项目管理标准的准确项目文档。
- 监控研究生命周期中的范围、时间表和财务表现。
- 支持财务监督，包括预测、预算跟踪、支出分析和发票审批。
- 主持内部和客户会议，确保明确的议程、记录的决策和可操作的后续行动。
- 同时处理多个研究，同时保持合规性、质量和运营卓越。
- 支持部门和客户
查看英文原文
Job Title: Labs Project Manager I
Job Location: Remote, United Kingdom
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Drive Clinical Innovation. Deliver Scientific Excellence.
At Thermo Fisher Scientific, you’ll join a global organization at the forefront of clinical research and laboratory science. In partnership with PPD, we support the world’s leading pharmaceutical and biotech organizations—successfully delivering over 2,700 clinical trials across 100+ countries in the past five years.
We are seeking a Project Manager – Labs to lead and coordinate central laboratory activities across clinical trial programs. This is a high-impact role requiring strong operational oversight, cross-functional leadership, and client engagement.
The Role: The Project Manager serves as the primary liaison between operational departments, affiliates, sponsors, and laboratory teams. You will oversee study setup, maintenance, and close-out activities for assigned clinical protocols and programs, while supporting the broader Project Management function.
Key Responsibilities:
- Serve as the primary project management lead for assigned clinical trials, including complex, multi-faceted studies.
- Act as the main point of contact for internal laboratory functions and external clients.
- Independently identify, manage, and mitigate study-level risks; escalate cross-functional or significant issues as needed.
- Lead study start-up activities including protocol and amendment review, milestone planning, risk assessments, and budget oversight.
- Coordinate cross-functional teams across laboratory operations, logistics, data management, quality, IT, and external vendors to ensure seamless execution.
- Manage study timelines, deliverables, interdependencies, and performance metrics to ensure on-time and high-quality data delivery.
- Maintain accurate project documentation in alignment with SOPs and project management standards.
- Monitor scope, timelines, and financial performance throughout the study lifecycle.
- Support financial oversight including forecasting, budget tracking, burn analysis, and invoice approvals.
- Lead internal and client-facing meetings, ensuring clear agendas, documented decisions, and actionable follow-ups.
- Balance multiple concurrent studies while maintaining compliance, quality, and operational excellence.
- Support departmental and client objectives through additional project-related responsibilities as required.
Required Education & Experience:
- Bachelor’s degree (or equivalent qualification).
- 2–4 years of experience in project management, laboratory operations, clinical research, or a related field.
*Equivalent combinations of education, training, and relevant experience will be considered.
Required Knowledge, Skills & Capabilities:
- Proven ability to manage multiple complex studies in a fast-paced, matrixed environment.
- Strong project management competencies including planning, execution, risk management, and stakeholder communication.
- Solid understanding of clinical trial processes and central laboratory operations.
- Analytical and solution-oriented mindset with sound decision-making capability.
- Proficiency in project management tools, internal systems, and standard business software.
- Ability to interpret and apply SOPs, work instructions, and regulatory requirements.
- Strong interpersonal and cross-functional collaboration skills.
- High degree of professionalism and discretion when handling confidential clinical and business information.
- Ability to perform effectively under pressure and manage competing priorities.
Working Environment:
At Thermo Fisher Scientific, employee wellbeing is a priority. We foster a supportive environment that enables individuals to thrive both professionally and personally.
- Work is performed in laboratory and/or clinical environments, with exposure to standard office equipment.
- Occasional travel and site visits may be required.
Why Join Thermo Fisher Scientific?
When you join us, you become part of a global organization committed to enabling customers to make the world healthier, cleaner, and safer. You’ll collaborate with industry-leading experts, contribute to groundbreaking clinical research, and grow within an environment that values innovation, accountability, and continuous development.
If you’re ready to lead complex clinical laboratory projects and make a measurable impact, we encourage you to apply.
Apply today and help deliver tomorrow’s breakthroughs!
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Originally posted on Himalayas