Study Start Up Manager, IQVIA Biotech
hace 6 días
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 the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities and oversight of the scope of work, budget and resources. Essential Functions Oversee the execution of Site Activation (including pre-award/bid defense activities) and/or Maintenance for assigned projects in accordance with the agreed RSU site activation strategy, adhering to project timelines. Develop, implement and maintain the Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required. Ensure collaboration across Regulatory & Site Activation, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the RSU Management scandal. Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com #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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FSP - Regulatory and Start Up Specialist
hace 1 semana
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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Global Study Grant
hace 1 semana
Mexico City IQVIA LLC A tiempo completoA global leader in clinical research is seeking a Study Grant Manager in Mexico City. In this full-time role, you will develop the global contracting strategy and oversee start-up contracting activities for select sponsors. The ideal candidate will have a Bachelor's degree and at least 5 years of relevant experience in clinical site contracting,...
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FSP - Regulatory and Start Up Specialist
hace 1 semana
Mexico City IQVIA A tiempo completoFSP - Regulatory and Startup Specialist Join to apply for the FSP - Regulatory and Startup Specialist role at IQVIA. Job Overview This position will be responsible for participating in end-to-end site management from feasibility to site closure, serving as a point of contact for investigative sites and the study team members. This includes supporting site...
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FSP - Regulatory and Start Up Specialist
hace 1 semana
Mexico City IQVIA A tiempo completoFSP - Regulatory and Startup Specialist Join to apply for the FSP - Regulatory and Startup Specialist role at IQVIA. Job Overview This position will be responsible for participating in end-to-end site management from feasibility to site closure, serving as a point of contact for investigative sites and the study team members. This includes supporting site...
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Study Grant Manager
hace 1 semana
Mexico City IQVIA LLC A tiempo completoStudy Grant Manager page is loaded## Study Grant Managerlocations: Mexico City, Mexicotime type: Full timeposted on: Posted Todayjob requisition id: R1522211Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the...
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Clinical Study Start-Up Associate
hace 1 semana
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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Site Activation
hace 4 días
Mexico City IQVIA A tiempo completoA 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...
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Regulatory Submissions Coordinator
hace 1 semana
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...