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88,000+ live jobsRemote, Madrid·Full-time·Added 8 days ago
Still open when we checked on 4 Oct
3 open roles
Full-time
Per the ad.
Fully remote
Per the ad.
Have the right to work in Spain
Worldwide Clinical Trials doesn't mention sponsorship in the ad.
Work in English
English is required, per the ad.
Have 3+ years of experience
Mid-level role.
University degree
“Bachelor's Degree or equivalent in business administration, finance, law, science or related field” — per the ad.
Site Contracting is 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.
Worldwide Clinical Trials (WCT) is a global, full-service contract research organization (CRO) that partners with pharmaceutical and biotechnology companies to conduct clinical trials and bring new therapies to market. With over three decades of experience, they provide a comprehensive range of services including clinical operations, biostatistics, regulatory consulting, and medical affairs. The company has a significant global footprint, with operations across North America, Europe, and Asia, employing thousands of professionals dedicated to advancing healthcare.
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.
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!
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.
A Senior Clinical Research Associate will manage site qualification, monitoring, and study close-out visits. The role offers a remote working arrangement within a global CRO.
This role manages the coordination and technical aspects of oncology clinical trials from start-up to closeout. It offers the chance to work within a global CRO focused on life-improving research.
Remote, Barcelona, Bilbao, Madrid, Seville, Valencia, A Coruña & Pamplona
