Experienced Study Start Up Specialist
hace 1 semana
Join Medpace at our Mexico City office As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining vital experience in study start up You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with Regulatory Submissions Coordinators, you will gain valuable hands on experience to enable you to develop a career in clinical research. Responsibilities Provide day-to-day departmental/project support activities, such as collection of vital documents for ethics submissions and preparation of study documents to competent authorities; Support Regulatory Submission Managers and Start Up teams in ensuring deadlines are adhered to; Conduct quality control of documents; Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements; and Perform other tasks as needed. Qualifications Bachelor's degree is required (preferably in a Life Sciences field) 1-3 years of regulatory submissions / study start up experience preferred; Ability to work in office; Excellent organizational and prioritization skills; Knowledge of Microsoft Office; Great attention to detail and excellent oral and written communication skills; and Fluency in spoken and written English. We kindly ask to submit applications in English. 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. 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 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 Perks 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 based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. #J-18808-Ljbffr
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Study Start Up Manager
hace 2 semanas
Mexico City Medpace A tiempo completoStudy 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...
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Study Start Up Manager
hace 2 semanas
Mexico City Medpace A tiempo completoStudy 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...
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Clinical Study Start-Up Associate
hace 6 días
Mexico City ICON A tiempo completoA leading clinical research organization is seeking a Site Management Associate in Mexico City. The successful candidate will manage study start-up activities, including trial administration and document management. A Bachelor's degree in life sciences is required. Candidates should possess strong organizational and communication skills, with at least 2...
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Regulatory Submissions Coordinator
hace 6 días
Mexico City Medpace A tiempo completoA clinical research organization in Mexico City is seeking a Regulatory Submissions Coordinator to support Regulatory Submissions and gain vital experience in study start-up. Responsibilities include providing support activities, ensuring compliance, and conducting document quality control. Requirements include a Bachelor's degree in Life Sciences, 1-3 years...
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Regulatory Start-Up Lead – LATAM Trials
hace 2 semanas
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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LATAM Regulatory Start-Up Lead for Trials
hace 6 días
Mexico City Medpace A tiempo completoA leading clinical research organization is seeking an experienced Regulatory Submissions Manager for a full-time, office-based role in Mexico City. 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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FSP - Regulatory and Start Up Specialist
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Mexico City IQVIA LLC A tiempo completoFSP - Regulatory and Start Up Specialist page is loaded## FSP - Regulatory and Start Up Specialistlocations: Mexico City, Mexicotime type: Full timeposted on: Posted Todayjob requisition id: R1520119**Job Overview**This position will be responsible for participating in end-to-end site management from feasibility to site closure, serving as a **point...
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Mexico City ICON A tiempo completoTW-FSP-SMA-Client office based with flexible WFH 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 Management...
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Study Start Up Associate
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Mexico City ICON A tiempo completoTW-FSP-SMA-Client office based with flexible WFH 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 Management...
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Centralized Study Specialist I
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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...
