CONTRACT SPECIALIST

Contract Specialist - This position will report to the LatAm Senior Contract Manager and will play a key role in the study start-up and clinical trial management processes at Medpace. The Contract Specialist will play a key role in advancing 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. ResponsibilitiesPrepare, negotiate, track and finalize the Confidentiality Agreements (CDA), Clinical Trial Agreements (CTA), Budgets and Letters of Indemnification (LOI) as well as Amendments to these documents, as needed. Manage all required contractual agreements with investigator sites, including distribution, negotiation of budget and language, tracking and finalization. Proactively identify site contract related risks and potential roadblocks. Prepare contract approval timelines with investigators and lead efforts to obtain contract approval to meet study deliverables. Maintain communication with project team and sites regarding status of all contractual requirements. Collaborate with the project team to ensure the client deliverables and expectations are achieved. Liase with internal customers to review contract or budget areas that impact final execution of site contracts. Maintain tracking regarding site contracts and provide regular updates as agreed by the study team to the project team and client regarding status and efforts to ensure timelines are maintained. QualificationsBachelors degree in business administration, legal studies, or life sciences. Ability to work with internal and external customers/vendors to meet project-specific goals. Ability to manage high volume work and meet rigorous deadlines. Flexibility to strategically manage negotiations with minimal oversight. Ability to interact with site and other functional areas as secondary project contact for contracting issues and questions. Ability to manage time and project requirements based on study deliverables. CRO experience or investigator site experience negotiating site agreements preferred. Fluency in English. Portuguese desirable. ***We kindly ask to send applications in English & salary expectation in BRL*** Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work weve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives AwardsRecognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets #J-18808-Ljbffr