Descripción de la oferta
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. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.Site Contract Department OverviewSite 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.What You Will DoPrepare country contract templates.Draft and send Site Agreements or any contracts associated to sites to begin negotiations.Negotiate contract language and budget 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 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.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 RoleProficient 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 ExperienceBachelor's Degree or 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, along with proficiency in either Spanish, French, Polish, or German.Proficiency with MS Word, Excel and Outlook.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.
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