Study Start Up Manager
hace 10 horas
Study Start Up Manager Join Medpace as a full‑time, office‑based Regulatory Submissions Manager in Mexico City. This role plays a key part in the study start‑up process, building on your experience in clinical trials and regulatory submissions. You will use your expertise to develop and grow your career while supporting our LATAM clinical trial activities. Responsibilities Efficiently manage and successfully execute all aspects of global start‑up. Perform quality checks on submission documents and site essential documents. Prepare and approve informed consent forms. Review pertinent regulations to develop proactive solutions to start‑up issues and challenges. Present during bid defenses, general capabilities meetings, and audits. Qualifications Submit your CV in English. Minimum education: bachelor’s degree in a life science major. At least 4 years of regulatory submissions/start‑up management experience, leading regulatory/start‑up project teams. Knowledge and experience of Clinical Trial Applications within Latin America. Strong oral and written communication skills. Team‑oriented approach and strong leadership skills. Willing to work in an office‑based model. Fluency in English and the local language. Company Overview Medpace is a full‑service clinical contract research organization (CRO) providing 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 a scientific and disciplined approach. With expertise across oncology, cardiology, metabolic disease, endocrinology, central nervous system, and anti‑viral and anti‑infective areas, Medpace is headquartered in Cincinnati, Ohio and employs more than 5,000 people in nearly 40 countries. Why Medpace? People, purpose, and passion drive our impact. Over the past 30+ years, we have positively impacted the lives of patients and families facing a wide range of diseases. Our work today shapes the future of healthcare. Perks & Benefits 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. Awards Recognized 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. Next Steps Your application will be reviewed, and if we are interested, a team member will contact you with details about next steps. Referrals increase your chances of interviewing by two times. #J-18808-Ljbffr
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Regulatory Start-Up Lead – LATAM Trials
hace 10 horas
Mexico City Medpace A tiempo completoA leading clinical research organization in Mexico City is seeking an experienced Regulatory Submissions Manager for a full-time, office-based role. This position is crucial for the study start-up process, requiring a bachelor's degree in life sciences and at least 4 years of relevant experience. Candidates should be fluent in English and the local language...
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Centralized Study Specialist I
hace 10 horas
Mexico City MEX Fortrea Clinical Development Mexico A tiempo completoAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
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Centralized Study Specialist I
hace 7 horas
Mexico City MEX Fortrea Clinical Development Mexico A tiempo completoAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
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Study Delivery Manager
hace 4 semanas
Mexico City ICON Strategic Solutions A tiempo completoJoin to apply for the Study Delivery Manager role at ICON Strategic Solutions. 1 day ago – Be among the first 25 applicants. Home – Based – Mexico. ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment, driving innovation and excellence, and we welcome you to join us...
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Study Delivery Manager
hace 4 semanas
Mexico City ICON Strategic Solutions A tiempo completoJoin to apply for the Study Delivery Manager role at ICON Strategic Solutions. 1 day ago – Be among the first 25 applicants. Home – Based – Mexico. ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment, driving innovation and excellence, and we welcome you to join us...
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Senior Global Contract Negotiator
hace 3 semanas
Mexico City IQVIA LLC A tiempo completoA leading clinical research firm in Mexico City is seeking a Contract Specialist to develop global contracting strategies and support start-up activities. The ideal candidate should have at least 5 years of experience in clinical site contracting, with strong negotiating and communication skills. Responsibilities include collaborating with sponsors,...
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Study Site Specialist
hace 3 semanas
Mexico City ICON A tiempo completoHome Office - Mexico ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Site Activation Lead to join our diverse and...
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Study Site Specialist
hace 3 semanas
Mexico City ICON A tiempo completoHome Office - Mexico ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Site Activation Lead to join our diverse and...
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Study Delivery Manager
hace 3 semanas
Mexico City ICON A tiempo completoHome - Based - Mexico ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Trial Manager to join our diverse and...
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Study Delivery Manager
hace 3 semanas
Mexico City ICON A tiempo completoHome - Based - Mexico ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Trial Manager to join our diverse and...
