Supply Chain Specialist

Our activities in LATAM are increasing rapidlyWe are currently seeking a full-time office based Supply Chain Specialist - CRO Logistics to join our team in Mexico City.This position will work on a team to accomplish tasks and projects that are instrumental to the company's success.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.ResponsibilitiesManage and maintain Import & Export activities and vendors (including brokers) for a clinical trial project in a country and/or region according to the scope contracted and timelines agreed; This includes frequent communication with exporters, brokers, customs, couriers and regulatory/clinical teams; Obtain the necessary information from client and vendors/exporters that supports the Import License application and approval process; Support the Regulatory Submission team by reviewing the initial CTA application to ensure appropriate study supplies are listed and complies with Import & Export local practices & regulation; Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements on Import & Export processes in the region; Review pertinent regulations and guidance, including updates, to develop proactive solutions to Import & Export issues and challenges in the region; andUtilize andassist in maintaining the Internal tracking system and/or other department trackers with Import & Export documentation, submission, approval and expiration dates.QualificationsBachelor's degree required, preferably in a business or life science field; Fluent written and verbal English; Demonstrate time management and professional oral and written communication skills; Demonstrated ability to think critically, independently, and exercise good judgement.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 6,000 people across 40+ countries.Why Medpace?People.Purpose.Passion.Make a Difference Tomorrow.Join Us Today.The work we've 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.Medpace PerksFlexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesAwardsRecognized by Forbes as one of America's Most Successful Midsize Companies in ****, ****, **** and ****Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibilityWhat to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.***Please submit CV in English***#J-*****-Ljbffr