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TMF运营专员II

雇主

Lifelancer

地点

远程 · 美国

待遇

$面议

工作模式

远程

截止日期

12月5日

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岗位摘要

Job Title: Associate II, TMF Operations Job Location: Virtual Argentina Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe.

岗位职责

Job Title: Associate II, TMF Operations
Job Location: Virtual Argentina
Job Location Type: Remote
Job Contract Type: Full-time
Job SeniorityLevel:
Who we are
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
Job Description
What Records Management Compliance Department does at Worldwide
TMF Operationshandles the processing, maintenance and archiving of all essential documents in strict accordance with pertinent Standard Operating Procedures, country-specific regulations, and industry best practices. Throughout Worldwide Clinical Trials, our culture of collaboration and innovation is what propels us in our pursuit of excellence in clinical research and making a meaningful impact on every patient's life. Roles within our TMF Operations department have a global scope, with the opportunity to regularly collaborate with members of the Worldwide Project Team.
What you will do
Fulfil the "TMF Approver" and/or "TMF QC Reviewer" roles as defined by the relevant Standard Operation Procedure(s) (SOP) and working practices.
Process, review, and resolve rejected Trial Master File (TMF) documents, for complex studies or Sponsor portfolio of studies both in an electronic and hard copy format.
Prepare periodic TMF Quality Control checklists for review by Project Team review.
Perform periodic TMF Quality Control to ensure adherence to regulatory, ICH GCP, Sponsor, and industry best practices.
Work with a variety of Electronic Document Management and electronic TMF Systems to review, classify and process Essential Documents
What you will bring to the role
Possess data collection, indexing and editing skills, including ability to adhere to standardized document naming conventions
Possess excellent written and verbal communication skills to clearly and concisely present information
Display strong interpersonal skills in a fast-paced, deadline oriented, rapidly changing environment
Handle multiple, highly detailed tasks with exceptional accuracy. Demonstrate strong planning and organizational skills
Demonstrate proficiency in Microsoft Word and Excel
Develop proficiency in use of an electronic document repository or eTMF. General understanding of clinical research principles and processes
Your experience
University Degreepreferred (Life Science desirable)
Up to 1-2 years of relevant TMF experience within the CRO/Pharma industry
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit or connect with us on LinkedIn.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
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

申请条件

- 具备临床试验文件管理(TMF)或相关记录管理经验
- 熟悉标准操作程序(SOP)及行业最佳实践
- 理解并遵守国家特定法规和监管要求
- 注重细节,具备高度的准确性和组织能力
- 能够处理、维护和归档基本文件
- 具备良好的协作和沟通能力,能与全球项目团队合作
- 熟练使用相关软件和电子文档管理系统
- 具备英语工作能力(因岗位为虚拟阿根廷,可能需英语或西班牙语)
- 全职工作承诺,适应远程办公环境

雇主简介

CVS Health是一家提供医疗健康服务和健康保险的综合性公司,致力于通过创新和关怀改善个人和社区的医疗体验。

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数据来源:Himalayas

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