Senior Specialist, Site Contracts - Spain

WCT Clinical Research Spain, S.L.; Madrid; Híbrido; EUR 60.000 - 75.000; Jornada completa

Descripción de la vacante

Worldwide underlines a Senior Site Contracts Specialist role in Madrid, focusing on end-to-end site contract management, negotiation of site budgets, and collaboration with study teams and the Worldwide Legal Department.

You will liaise with investigators and vendors, ensure regulatory compliance, and support SOP improvements while coordinating with legal, finance, data protection and clinical operations teams.

Formación

• Experience negotiating complex contract terms with clinical sites and vendors.
• Strong knowledge of ICH-GCP and local regulatory requirements.
• Ability to explain complex contract terms clearly and concisely.

Responsabilidades

• Act as a Subject Matter Expert (SME) on Clinical Trial Agreement processes at country and site level.
• Preparation, negotiation and finalization of site contracts and budgets.
• Manage the Investigator Budget and liaise for contract communications.
• Review and finalize Clinical Trial Agreements and related documents for completeness and accuracy.

Conocimientos

Contract negotiation

Regulatory knowledge

Cross-functional collaboration

Leadership

Educación

Bachelor's degree or equivalent

Herramientas

MS Word

Excel

Outlook

Descripción del empleo

Who we are

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

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

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 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

• Act as a Subject Matter Expert (SME) on Clinical Trial Agreement processes at country and site level
• Preparation, negotiation and finalization of site contracts and budgets
• Manage the Investigator Budget and act as a key liason for contract related communications
• Resolve negotiation issues and escalating risks, drive process for improvements, contribute to SOP develoment and keep templates updated
• Liaising and collaborating with Worldwide stakeholders as well as external stakeholders (such as sites, investigators etc.)
• Review and finalize Clinical Trial Agreements and/or any document associated including site budget, for completeness and accuracy

What you will bring to the role

• Mastery in negotiating complex contract terms with clinical sites and vendors
• In-depth understanding of international and local regulatory requirements for clinical trials (e.g., FDA, EMA, ICH‑GCP).
• Ability to explain complex contract terms clearly and concisely
• Leadership skills to guide and support junior contract specialists
• Ability to collaborate effectively with cross‑functional teams, including but not limited to legal, finance, data protection and clinical operations.

Your experience

• 3- 4 years of experience as a Senior Site Contracts Specialist or minimum 5 years Site Contract experience in Clinical Research Pharmaceutical or CRO industry
• Bachelor's Degree or equivalent in business administration, finance, law, science or related field
• Proficiency with MS Word, Excel and Outlook
• Knowledge and understanding of ICH and GCP Guidelines, as well as local country legislation in the sphere of clinical trials and local regulatory requirements.
• Adept knowledge of biopharmaceutical/CRO industry and applicable local regulatory requirements

We love knowing that someone is going to have a better life because of the work we do. 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.

This is who we are. We’re a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever. We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we’re here, you’ll get a different answer. And that’s what makes us special.