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日本现场合同专员 - 远程

雇主

Worldwide Clinical Trials

地点

远程 · 美国

待遇

$面议

工作模式

远程

截止日期

12月6日

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岗位摘要

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

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 the Site Contract department does at Worldwide
Site Contractingis an essential function within any CRO, and our seasoned team spans decades of experience within the industry and possesses robust legal experience as well. The department is responsible for reviewing, analyzing, and drafting clinical research site contracts, investigator contracts and other project-related contracts. Our global team is familiar with the specific laws for the countries and sites we occupy. We negotiate and finalize clinical trial contracts and services contracts with the Worldwide Legal Department, study teams, Sponsors, investigators, and/or clinical sites.
What you will do
Prepare country contract templates;
Draft and send Site Agreements or any contracts associated to sites to begin negotiations;
Negotiate contract(s) language and budget(s) with each assigned site to finalization / execution;
Review study budgets and costs pertaining to contract negotiation;
Perform quality check of Site Agreements or any documents associated before signature process starts;
Liaise with Worldwide Legal Department, Data Privacy team, study teams, Sponsor, sites, investigators etc.
Send Fully Executed Site Agreementsor any document associated to: site, eTMF, payment team, Sponsor, post to internal Sharepoint, as applicable;
Negotiate Site Agreements Amendmentlanguage and budget with sites;
Create termination letter or any other type of documents related, and send to sites for signature, as applicable;
Maintain tracking tool with live/real-time/regular updates for functional activities;
What you will bring to the role
Proficient in negotiating contract terms with clinical sites and vendors.
Ability to identify and address contract issues and disputes efficiently.
Good understanding of international and local regulatory requirements for clinical trials (e.g., FDA, EMA, ICH-GCP).
Solid analytical skills to review and interpret contract terms and financial data.
Ability to identify risks and develop mitigation strategies.
Your experience
Bachelor's Degreeor equivalent in business administration, finance, science or related field.
1 to 3 years of experience in Clinical Research Pharmaceutical or CRO industry working with investigator/site contracts or related legal field.
Excellent verbal and written English and Japansese.
Proficiency with MS Word, Excel and Outlook.
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.
Originally posted on Himalayas

申请条件

- 具备合同起草、审查和谈判经验,特别是临床试验或研究相关合同
- 熟悉临床研究行业及CRO环境下的合同流程
- 了解不同国家或地区的法律要求,能适应全球合同管理
- 拥有法律或相关领域的扎实背景,具备法律分析能力
- 能与内部团队(法律、研究、赞助商)及外部机构有效协作
- 注重细节,具备优秀的书面和口头沟通能力
- 能独立处理多项任务并推动合同谈判至最终确定
- 具备团队合作精神,适应多元化和包容性工作环境

雇主简介

Worldwide Clinical Trials is a global midsize CRO providing clinical research services, with a team of over 3,500 experts, focused on innovative approaches to advance treatments for persistent diseases.

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数据来源:Himalayas

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