Senior Specialist, Site Contracts – UK Negotiations

Posted Sep 14

This is a fully remote position, open to applicants in Spain, +6 more countries.

πŸ“‹ Description

β€’ Prepare templates for country-specific contracts.

β€’ Draft and distribute Site Agreements and other site-related contracts to initiate negotiations.

β€’ Conduct negotiations on contract terms and budgets with assigned sites until finalization and execution.

β€’ Review study budgets and expenses associated with contract negotiations.

β€’ Execute quality checks on Site Agreements and related documents prior to signing.

β€’ Provide either draft or signed contracts and budgets to regulatory teams for submission upon request.

β€’ Collaborate with the Worldwide Legal Department, Data Privacy team, study teams, Sponsors, sites, and investigators.

β€’ Facilitate contract signatures by Worldwide when necessary.

β€’ Distribute fully executed Site Agreements and related documents to sites, eTMF, payment teams, Sponsors, and internal SharePoint.

β€’ Negotiate amendments to Site Agreements and budgets with sites.

β€’ Generate termination letters and other relevant documents, sending them to sites for signatures.

β€’ Maintain tracking tools with live, real-time, or regularly updated functional activity logs.


⛳️ Requirements

β€’ Bachelor's Degree or equivalent in business administration, finance, science, or a related field.

β€’ 3 to 5 years of experience in the Clinical Research, Pharmaceutical, or CRO industry, specifically working with investigator/site contracts or a related legal field.

β€’ Experience in negotiating with UK sites is essential.

β€’ Exceptional verbal and written communication skills in English and the local language.

β€’ Proficient in MS Word, Excel, and Outlook.

β€’ Skilled in negotiating contract terms with clinical sites and vendors.

β€’ Capable of identifying and efficiently addressing contract issues and disputes.

β€’ Strong understanding of international and local regulatory requirements for clinical trials, including FDA, EMA, and ICH-GCP.

β€’ Solid analytical skills for reviewing and interpreting contract terms and financial data.

β€’ Ability to identify risks and formulate effective mitigation strategies.


🏝️ Benefits

β€’ Equal employment opportunities irrespective of protected characteristics.

β€’ A diverse and inclusive work environment.

β€’ Supportive and collaborative team structures.

β€’ Accessible leadership.

β€’ Opportunities for employee success and professional development.

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