.Job Summary:Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Contract Specialist to join our LatAm Site Contract Team within the Clinical Operations team. 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.Responsibilities:- Is responsible for preparing, negotiating, tracking and finalizing the Confidentiality Agreements (CDA), Clinical Trial Agreements (CTA), Budgets and Letters of Indemnification (LOI) as well as Amendments to these documents, as needed.- Manages all required contractual agreements with investigator sites. This includes distribution, negotiation of budget and language, tracking and finalization.- Proactively identifies site contract related risks and potential roadblocks.- Prepares contract approval timelines with investigators and leads efforts to obtain contract approval to meet study deliverables.- Maintains communication with project team and sites regarding status of all contractual requirements.- Collaborates with the project team to ensure the client deliverables and expectations are achieved.- Liaises with internal customers to review contract or budget areas that impact final execution of site contracts.- Maintains tracking regarding site contracts and provides regular updates as agreed by the study team to the project team and client regarding status and efforts to ensure timelines are maintained.Qualifications:- Bachelors 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 mínimal 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.Medpace Overview:Medpace 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
