出海雷达

助理经理/经理,项目服务 - 实验室(远程 - 东部)

Associate Manager / Manager, Project Services - Laboratories (Remote - East

职能支持限定地区(需当地身份)
公司Lifelancer
薪资$64,200 - $173,000/年
工作地点United States
地域资格限定地区(需当地身份)
时区要求日间重叠约 9 小时,基本正常作息
用工类型Full Time
发布时间11 天前
数据来源Himalayas
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注意地域限制:该职位明确限定在 United States 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。

职位名称:高级经理/经理,项目服务 - 实验室(远程 - 东部时间)
工作地点:马萨诸塞州波士顿,美国
工作地点类型:远程
工作合同类型:全职
职位级别:
我们正在寻找有经验的实验室专业人员加入IQVIA实验室的项目服务团队。
该职位为100%远程工作(东部时间工作时间)。我们在多个级别招聘——候选人将根据经验匹配到合适的级别。
我们招聘充满热情的创新者,通过深思熟虑和包容性的协作推动医疗保健发展。如果您希望发现一份更有意义的职业,加入我们,共同推动研究和开发的变革与加速。
职位概述:
在一般指导下,管理客户或特定项目的实验室各个方面,从项目授标到启动、维护和结项,作为主要联系人。领导计划、沟通、风险管理及跨职能协调,以实现高质量、以客户为中心的执行。
您将负责的工作:

  • 管理指定的临床试验实验室项目,从授标到结项,确保理解并应用方案要求
  • 领导研究启动活动,包括方案和预算审查、启动会议以及项目和风险管理计划的实施
  • 监控时间表、交付成果、指标和预算,包括趋势分析、范围变更和变更订单
  • 作为赞助商的单一联系人,主导客户沟通、会议以及问题分类和升级
  • 推动及时、以客户为中心的问题解决,并协调跨职能资源以消除研究障碍
  • 监督特定方案的实验室指导文件的开发和实验室规格的维护
  • 支持提案开发、投标防御准备以及赞助商或项目特定的标准和程序的开发
  • 记录经验教训,并支持项目和项目的持续改进

我们寻找的人才:

  • 生命科学及相关领域的学士学位优先
  • 在受监管的实验室环境中3年以上经验
  • 2年以上项目管理经验(例如:研究启动、方法验证或转移、客户项目)——不要求正式的项目管理职位名称
  • 熟练使用微软办公软件(Word、Excel、PowerPoint)
查看英文原文

Job Title: Associate Manager / Manager, Project Services - Laboratories (Remote - East
Job Location: Boston, Massachusetts, United States of America
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
We are seeking experienced laboratory professionals to join the Project Services team at IQVIA Laboratories.
This role is 100% remote (Eastern Time business hours). We are hiring at multiple levels — candidates are aligned to the appropriate level based on experience.
We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.
Job Summary:
Under general direction, manage all laboratory aspects of clinical trial projects for a client or a specific program, serving as the primary point of contact from award through start-up, maintenance, and closeout. Lead planning, communication, risk management, and cross-functional coordination to deliver high-quality, customer-focused execution.
What You'll Be Doing:

  • Manage assigned clinical trial laboratory projects from award through closeout, ensuring protocol requirements are understood and applied
  • Lead study set-up activities including protocol and budget review, start-up meetings, and implementation of project and risk management plans
  • Monitor timelines, deliverables, metrics, and budgets, including trend analysis, scope changes, and change orders
  • Serve as the single point of contact for sponsors, leading client communications, meetings, and issue triage and escalation
  • Drive timely, customer-focused problem solving and coordinate cross-functional resources to remove study obstacles
  • Oversee development of protocol-specific laboratory instructional documents and maintenance of laboratory specifications
  • Support proposal development, bid defense preparation, and development of sponsor or program-specific standards and procedures
  • Capture lessons learned and support continuous improvement across projects and programs

What We Are Looking For:

  • Bachelor's Degree in Life Sciences and/or related field preferred
  • 3+ years of experience in a regulated laboratory environment
  • 2+ years of experience managing projects (e.g., study setup, method validation or transfer, client programs) — a formal project management title is not required
  • Demonstrated computer proficiency with Microsoft Office (Word, Excel, PowerPoint) and comparable company systems in a project delivery environment

The Knowledge, Skills and Abilities Needed for This Role:

  • Strong interpersonal and client management skills, with the ability to interact effectively with sponsor stakeholders
  • Experience with Lab Trial Management Systems (LTMS)
  • Strong organizational skills with high accuracy and attention to detail while managing multiple priorities and deadlines
  • Strong written and verbal communication skills with good command of English and clinical research terminology
  • Ability to work effectively in a fast-paced, high-stress environment with a customer-focused mindset
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients

What We Offer You:
We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.
To learn more about our benefits, visit
If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $64,200.00 - $173,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

This job is curated by Lifelancer.
Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.
Please apply via Lifelancer platform to get connected to the application page and to find similar roles.
Originally posted on Himalayas

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