Principal Site Contract Specialist - Europe - Remote

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 almost 2,500 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.

What you will do

• Serves as a Lead and subject matter expert on Clinical Trial Agreement processes at project level.
• Develops and provides expert and strategic pathways for the successful site contract execution within a project/program.
• Supervises and mentors allocated Site Contracts Specialist, ensuring effective planning, effective communication, on time issues escalation, problem solving and execution.
• Agrees and negotiates Clinical Trial Agreements templates, fall back language and sites budget negotiation parameters with project lead and Sponsor.

 

 

 

What you will bring to the role

 

• Extensive knowledge regarding global requirements in regards to Clinical Trial Agreements requirements and negotiations.
• Extensive knowledge regarding Worldwide Site Contracts SOPs, WIs, internal tools and related processes.
• Ability to review and understand technical, medical and legal documents related to Clinical Trial Agreements.
• Excellent leadership skills with ability to work in fast-paced, deadline oriented, and changing environment

 

 

Your background

•  Bachelor's degree or equivalent in business administration, law, science or related field.
• Extensive knowledge regarding Worldwide Site Contracts SOPs, WIs, internal tools and related processes.
• Ability to review and understand technical, medical and legal documents related to Clinical Trial Agreements.
• Excellent leadership skills with ability to work in fast-paced, deadline oriented, and changing environment

 

 

Why Worldwide

At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every clinical trial like a patient’s life depends on it – because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.   

 

Interested in hearing more about Worldwide or our roles? Check out our careers page at www.worldwide.com/careers! 

 

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