Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based and hybrid Contract Specialist to join our Clinical Operations team in London. This position plays a key role in the study start-up and clinical trial management processes at Medpace. The Site Contract Specialist will advance the start-up of our projects. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Oversees negotiations of clinical study agreements (CSA''s) on a study level and drives CSA document finalization and execution, including contractual language and terms, financial attachments, and investigator grant budgets in collaboration with a global team of site contract and budget negotiators. Acts as first-line subject matter expert for all such CSA elements on assigned studies for internal stakeholders. Advises stakeholders on issue resolution within the context of assigned studies. Plans contract execution strategy for assigned studies-including forecast of site-specific contractual execution timelines with as much accuracy as possible and coordinates with internal study team stakeholders to ensure that CTA strategy is aligned with overall study start-up plans and expectations overall. Works closely with internal stakeholders to prepare site contractual templates, including payment terms, in order to drive successful negotiation ..... full job details .....