高级临床数据团队负责人
Senior Clinical Data Team Lead
职位名称：高级临床数据团队负责人
工作地点：印度远程办公
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）
工作环境条件
遵守所有良好生产规范（GMP）安全标准
职位描述
作为高级临床数据团队负责人加入我们——在创新的最前沿发挥作用
在过去五年中，我们已成功支持了全球前50强制药公司和750多家生物科技公司，覆盖100多个国家的2700多项临床试验。
作为我们专家团队的一员，你将有机会确保运营卓越，真正提升组织绩效。作为高级临床数据团队负责人，你将负责一个或多个项目的数据管理，并根据需要与项目负责人和/或客户进行沟通。
你将负责：
- 将项目方案的相关部分应用到日常任务中，并指导他人如何将其应用到自己的日常任务中。
- • 作为数据管理研究活动的跨部门和客户联络人。
- • 定期为管理层、项目负责人和/或客户提供特定项目的进度报告。
- • 监控和分析研究指标，并根据组织的风险管理流程进行升级。
- • 在需要时参与业务发展活动，协助准备投标文件，并在投标答辩会议中代表数据管理。
- • 协助项目工时预测和资源需求识别。
- • 协助项目预算监督，包括识别可能超出范围的工作并参与合同修改流程。
- • 领导高数量和高度复杂的研究。
- • 独立领导并分配任务，以确保项目活动按时、按质量、按预算完成。
- • 指导初级员工完成研究中的所有相关任务。
- • 协助对分配的项目进行行政和财务监督。
- • 向管理层汇报其研究中的所有数据管理活动。
教育和经验要求：
• 本科或同等学历及相关正式学术/职业资格
• 具有提供履行该职位所需知识、技能和能力的先前经验（相当于5年以上）。
在某些情况下，等同于由适当教育、培训和/或直接相关经验组成的组合。
查看英文原文
Job Title: Senior Clinical Data Team Lead
Job Location: Remote, India
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety StandardsJob 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).
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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Originally posted on Himalayas