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.

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?Our integral 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; Negotiate contract(s) language and budget(s) with each assigned site to finalization / execution; Review study budgets and costs pertaining to contract negotiation; If requested,provide draft/signed contract/budget to the regulatory team for submission purpose, where needed; 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, payment team, Sponsor, post to internal Sharepoint, as applicable; Negotiate Site Agreements Amendment language and budget with sites;

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 require?Solid analytical skills to review and interpret contract terms and financial data.

Your Experience

Bachelor's Degree or equivalent in business administration, finance, science or related field. 3 to 5 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 local language skills. Proficiency with MS Word, Excel and Outlook.

📌 Global Site Contracts Specialist (Málaga)
🏢 Worldwide Clinical Trials
📍 Málaga