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.
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 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 general 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 budgetsand 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 Agreements or any document associated to: site, eTMF,

📌 Site Contracts Specialist - Europe - Remote (Barcelona)
🏢 Worldwide Clinical Trials
📍 Barcelona