Experienced Clinical Safety Coordinator
hace 2 semanas
Our Latin American activities are growing rapidly, and we are currently seeking a full-time, office-basedClinical Safety Coordinator to join our team This position plays a key role in the pharmacovigilance process at Medpace. Working in 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. Responsibilities Oversight of submission of safety reports in the appropriate format to Competent Authorities/Ethics Committees in compliance with regulatory timelines. Regular interaction with other internal departments globally and locally, such as Clinical Operations, Data Management and Regulatory Submissions. Draft study specific safety documents as required. Work in a global team to distribute safety reports globally. Qualifications Bachelor’s degree in Life Science area required. Demonstrate fundamental knowledge of Good Clinical Practice (GCP) guidelines and medical terminology. Knowledge of Electronic Data Capture (EDC) systems and other clinical databases. Experience safety reporting to regulatory authorities in Spanish speaking LATAM countries. Drug safety experience. Knowledge of applicable safety reporting guidelines. Strong attention to detail. 3 years of experience working within drug safety. Fluency in Spanish & 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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LATAM Clinical Safety Specialist
hace 2 semanas
Mexico City Medpace A tiempo completoA clinical contract research organization seeks a full-time Clinical Safety Coordinator in Mexico City. This role involves oversight of safety report submissions and interaction with global departments. Candidates must have a Bachelor's in Life Sciences, drug safety experience, and fluency in Spanish and English. The position offers a competitive...
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Central Review Coordinator — Clinical Trials
hace 1 día
Mexico City ICON Clinical Research A tiempo completoA leading clinical research organization in Mexico is seeking a Central Review Coordinator to facilitate centralized review activities in clinical trials. Responsibilities include coordinating logistics, collaborating with teams, and ensuring compliance with protocols. Candidates should possess a Bachelor's degree in a relevant field and experience in...
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Senior / Lead Clinical Data Coordinator
hace 2 semanas
Mexico City ICON Clinical Research A tiempo completoSenior Clincal Data Coordinator 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. Lead/Senior Clinical Data Coordinator This is a hybrid role...
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Senior / Lead Clinical Data Coordinator
hace 2 semanas
Mexico City ICON Clinical Research A tiempo completoSenior Clincal Data Coordinator 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. Lead/Senior Clinical Data Coordinator This is a hybrid role...
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Lead Clinical Data Manager — Hybrid
hace 2 semanas
Mexico City ICON Clinical Research A tiempo completoA clinical research organization is seeking a Senior Clinical Data Coordinator in Mexico City. This hybrid role involves creating data management plans, resolving data discrepancies, and collaborating with cross-functional teams. Candidates should have a Bachelor's degree in Life Sciences or Healthcare and 5-7 years of experience managing clinical databases....
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Clinical Trial Operations Coordinator
hace 1 día
Mexico City ICON Clinical Research A tiempo completoA leading clinical research organization based in Mexico City seeks candidates for a role focused on data management and support for clinical trials. The successful applicant will perform tasks such as data entry, document management, and vendor support, requiring attention to detail and strong organizational skills. Candidates should have an Associate’s...
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Pharmacovigilance Lead – Post‑Marketing Safety
hace 2 semanas
Mexico City ICON A tiempo completoA leading clinical research organization in Mexico City seeks a Pharmacovigilance Coordinator. This pivotal role involves supervising safety monitoring of clinical trials and marketed products and ensuring adherence to global regulations. Ideal candidates will possess a Bachelor's in life sciences and experience in pharmacovigilance or drug safety. The...
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Centralized Study Specialist I — Clinical Systems Lead
hace 3 semanas
Mexico City MEX Fortrea Clinical Development Mexico A tiempo completoA global contract research organization is seeking an experienced Centralized Study Specialist I in Mexico City. This role involves managing clinical systems, supporting study documentation, ensuring compliance, and mentoring junior team members. The ideal candidate should have a degree in Life Sciences and 2-3 years of clinical research experience, with...
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Clinical Data Coordinator
hace 2 semanas
Mexico City ICON plc A tiempo completoClinical Data Coordinator IIThis is a hybrid role requiring 3 days in the office and 2 days working from home.Location: Mexico City - Insurgentes SurWhat you will be doing Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.Manage clinical and third-party data reconciliation based on edit...
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Clinical Data Coordinator
hace 1 día
Mexico City ICON plc A tiempo completoClinical Data Coordinator IIThis is a hybrid role requiring 3 days in the office and 2 days working from home.Location: Mexico City - Insurgentes SurWhat you will be doing Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.Manage clinical and third-party data reconciliation based on edit...
