Sr. Clinical Data Team Lead - Remote U.S
职位标题：高级临床数据团队领导 - 远程美国工作地点：拉利，北卡罗来纳州，美国工作场所类型：远程工作合同类型：全日制工作资深级别：工作时间表标准 （月-周五）环境条件办公室工作内容 加入我们作为高级临床资料团队负责人 创新前沿影响 我们已经成功支持了50家顶尖的药品公司和750多家生物技术，在过去5年中跨越100多个国家进行2,700项临床试验。作为我们的专业团队的一部分，你将有机会确保对组织绩效真正差异的运营卓越性。作为高级临床数据团队负责人，你将担任一个或多个项目的主要数据管理员，并根据需要与项目领导和/或客户保持联系。你所做的：· 将项目协议的相关组件应用于日常任务，并指导他人如何适用他们的日常任务。•在所有 DM 研究活动中，以部门间和客户之间的联系方式工作。•定期为管理人员，项目领导者和/或顾客提供项目具体状态报告。•监测和分析研究标准，并按组织风险管理流程进行升级。•可协助竞标辩护会议的招标准备和数据管理，如有必要。•帮助预测项目时间和确定资源需求。•协助监督项目预算，包括识别潜在的工作范围之外以及参与合同修改过程。•领导大量/高度复杂的研究。•独立负责并委托任务以确保项目活动及时完成项目的时间表，质量和预算。•指导初级层工作人员在一项研究中的所有相关任务上。•协助管理和财政监督分配项目。•与管理层沟通有关其研究中的所有数据管理活动。教育和经验要求：•学士学位或相当及相关的正式学术/职业资格 •提供工作执行知识，技能和能力的前体验 （相对于5年以上）. 前体验必须反映主要到终端) 的责任。在某些情况下，一个等级，由适当教育，培训和培训组成的组合
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Job Title: Sr. Clinical Data Team Lead - Remote U.S
Job Location: Raleigh, North Carolina, USA
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Join Us as a Senior Clinical Data Team Lead – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Senior Clinical Data Team Lead, you will act as a lead data manager for one or more projects and serve as a liaison to the Project Lead and/or client as required.
What You’ll Do:
- Applies relevant components of the project protocol to daily tasks and directs others on how to apply to their daily tasks.
- •Acts as an interdepartmental and client liaison for all DM study activities.
- •Produces project-specific status reports for management, Project Lead and/or clients on a regular basis.
- •Monitors and analyzes study metrics and escalates per the organization's risk management processes.
- •May participate in business development activities by assisting with bid preparation and representing data management at bid defense meetings, where required.
- •Assists with project forecasting of hours and identification of resource requirements.
- •Assists with the oversight of project budgets including identification of potential out of scope work and participation in the Contract Modification process.
- •Leads, high volume/highly complex studies.
- •Independently leads and delegates tasks to ensure timely completion of project activities to project timelines, quality and budget.
- •Mentors junior level staff on all associated tasks within a study.
- •Assists with administrative and financial oversight for allocated projects.
- •Communicates with management regarding all data management activities within their studies.
Education and Experience Requirements:
•Bachelor's degree or equivalent and relevant formal academic / vocational qualification
•Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years). Prior experience must reflect lead(end-to-end) responsibilities.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
- Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, SOPs and client expectations
- •Ability to use interactive computer programs
- •Good written/ verbal communication skills with a strong command of English language and grammar; good organizational, analytical/problem solving skills and attention to detail
- •Ability to work productively in both a team environment and independently as needed
- •Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
- •Strong customer focus and excellent interpersonal skills.
- •Ability to direct and train study team
- •Ability to act as a study or department expert for DM processes
- •Ability to support project resourcing and project timeline planning and adherence to timelines
Working Conditions and Environment:
•Work is performed in an office environment with exposure to electrical office equipment.
•Occasional drives to site locations with occasional travel both domestic and international.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.
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