Join Medpace in Mexico City!
We are currently seeking a full-time, office-based Clinical Research Project Coordinator to join our Clinical Trial Management team.
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.ResponsibilitiesEngage in clinical trial management on a day to day level; Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports; Interact with the Sponsor, study sites, and internal associates; Create and maintain project timelines; andCoordinate project meetings and produce quality minutes.QualificationsBachelor's degree in a health sciences field; Prior experience as a Study Coordinator or within the pharmaceutical industry preferred; Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills; andFluency in English.Medpace OverviewMedpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research.
We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective.
Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.Why Medpace?
When you join Medpace,



you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.Purpose-Driven WorkWork alongside physicians, scientists, and industry-leading experts committed to advancing the general development of medical therapeutics through clinical research excellenceCollaborative CultureContribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.Leadership throughout Medpace is both accessible and approachableContinuous Growth & DevelopmentOffice based environment with on-site mentorsDefined career paths with clear advancement opportunitiesIndustry renowned onboarding and training programs designed to accelerate professional developmentOngoing training and continuous learning opportunities throughout your careerAn environment that encourages employees to influence change, contribute ideas, and grow quicklyOther Employee BenefitsCompetitive compensation programs that recognize and reward performanceComprehensive health, wellness, retirement, and PTO benefitsOffice based culture with occasional WFH that provides flexibility for eligible positions after trainingCompany-sponsored social eventsPlease note benefits may vary based on country.What to Expect NextA Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview.
While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
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📌 Clinical Research Project Coordinator (Xico)
🏢 Medpace
📍 Xico