Senior Associate II, TMF Operations - EMEA/LATAM- Fixed term- Remote
职位名称：高级副官 II,TMF 运营 - EMEA/LATAM-固定任期-远程工作地点：虚拟克罗地亚，克罗地雅的工作地点类型：远程工作合同类型：全日制工作资深级别：高级副主任 II,TM F 运营 -EMEA/LATM-固定的任期-遥控 Req ID:JR101912发布：2026-07-08 雇用类型：全日制工作位置：远程办公地点：虚假克罗地亞，克罗的亚工作内容 我们是一个全球性中大型 CRO,超越界限，创新和发明，因为那些玩得安全的人并没有铺平了治愈世界上最持久疾病的道路。我们是全球临床试验，我们是一个由3500多名专家，聪明思想家，梦想家和执行者组成的全球团队，共同改变世界最好地体验 CRO 的方式。我们的使命是每天都以热情和目的努力改善生活，我们正在寻找那些重视同样的追求的人。为什么在全球范围内我们相信每个人都有重要作用来让患者及其护理人员的生活变得更美丽。从实践，可访问的领导者到团队，我们致力于让来自各个背景和经验的专业人士取得成功。我们优先培养多元化和包容性的环境，以继续促进合作和创造力。我们自豪地成为一个工作场所，人们通过自己做出最好的努力而成长，并受到每天最佳工作启发。加入我们！世界范围内 TMF 运营管理合规部门在严格遵守相关标准操作程序，法规和行业最佳做法的情况下处理，维护和存档所有必要记录。在全球临床试验中，我们的合作和创新文化推动我们追求临床研究卓越并对每个患者的生活产生有意义的影响.TMF 运营部门中的角色具有全球范围，有机会定期与世界项目团队成员合作。你将做什么？执行 RMC 领导活动，管理一系列复杂的研究或赞助商组合。直接与多个项目团队员和赞助商沟通以评估与 TMF 相关的项目的需求，并提供主题专业知识 (SME).
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Job Title: Senior Associate II, TMF Operations - EMEA/LATAM- Fixed term- Remote
Job Location: Virtual Croatia, Croatia
Job Location Type: Remote
Job Contract Type: Full Time
Job Seniority Level:
Senior Associate II, TMF Operations - EMEA/LATAM- Fixed term- Remote
Req ID: JR101912
Posted: 2026-07-08
Employment Type: Full Time
Work Location: Remote
Location: Virtual Croatia, Croatia
Job Description
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! What Records Management Compliance Department does at Worldwide TMF Operations handles the processing, maintenance and archiving of all essential records in strict accordance with pertinent Standard Operating Procedures, 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 Perform RMC Lead Activities, managing a number of complex studies or Sponsor portfolio of studies. Communicate directly with multiple Project Team members and Sponsors to assess project needs relevant to the TMF and to provide Subject Matter Expertise (SME). Oversee the Quality Control process including planning, reporting and follow up on non-compliance accordingly. Assist in development of project specific TMF Quality Management Documents. Prepare, maintain, and present TMF Key Performance Indicators and underlying data analysis trends with Project Teams and Sponsors. Support Regulatory and Sponsor audits and audit finding resolution, where necessary. What you will bring to the role Proficient understanding of clinical research principles, industry standards and regulations applicable to TMF Management Demonstrate strong planning and organizational skills with ability to work under pressure Display strong interpersonal skills in a fast-paced, deadline oriented, rapidly changing environment Possess excellent written and verbal communication skills to clearly and concisely present information to internal and external parties Ability to identify solutions and make decisions or have awareness to consult to find optimal regulatory compliant solutions including those required for complex technical situations. Your experience University degree preferred (Life Science desirable) A combination of education plus 2-4 years of relevant experience Knowledge of working within a highly regulated industry or experience of CRO/Pharmaceutical Company 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 www.Worldwide.com 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 is who we are. We’re a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever. We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we’re here, you’ll get a different answer. And that’s what makes us special. Not finding the right fit? 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About Worldwide Clinical Trials
Worldwide Clinical Trials is 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. We are a global team of over 3,500+ experts, bright thinkers, dreamers and doers.
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