Study Start Up Manager, IQVIA Biotech

IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture,-face and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster. Job Overview Direct and manage...

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...

Overview Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Mexico City. This position plays a key role in the study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop...

IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster. Manage and support the operational...

Associate Clinical Project Management Director, IQVIA Biotech page is loaded## Associate Clinical Project Management Director, IQVIA Biotechlocations: Mexico City, Mexicotime type: Full timeposted on: Posted Todayjob requisition id: R *IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all...

A leading biotech consulting firm in Mexico City is looking for a Site Activation Manager. This role entails overseeing site activation and maintenance activities, developing management plans, and ensuring compliance with project strategies. The ideal candidate will manage pre-award activities and coordinate with various stakeholders to achieve project scope...

A leading clinical research organization is hiring a Study Start Up Associate II in Mexico City for a hybrid position. You will support site partners in collecting and reviewing essential start-up submission packages while ensuring compliance with regulatory guidelines. The ideal candidate will have a Bachelor's Degree in Life Sciences and 2-4 years of...

A 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...

A leading clinical research organization in Mexico City is seeking a Regulatory Submissions Manager to oversee the start-up process for clinical trials. Candidates should have at least 4 years of relevant experience with strong communication and leadership skills. The role is office-based with a focus on managing global start-up activities and ensuring the...

A clinical research services provider in Mexico is seeking a professional to direct and manage the delivery of site activation and regulatory activities for clinical studies. The role involves overseeing project execution in compliance with strategy and timelines, ensuring collaboration across various teams, and maintaining management plans. The ideal...