Study Start Up Manager, IQVIA Biotech
hace 7 horas
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 #J-18808-Ljbffr
-
Study Start Up Manager
hace 7 horas
distrito federal, México 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...
-
distrito federal, México IQVIA A tiempo completoIQVIA 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...
-
distrito federal, México IQVIA LLC A tiempo completoAssociate 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...
-
Site Activation
hace 7 horas
distrito federal, México 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...
-
Regulatory Start-Up Lead – LATAM Trials
hace 7 horas
distrito federal, México 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...
-
distrito federal, México MSC Quintiles Mexico S. de R.L. de C.V. A tiempo completoIQVIA 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...
-
Study Start-Up Lead — Clinical Trial Activation
hace 7 horas
distrito federal, México IQVIA A tiempo completoA 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...
-
FSP - Sr. Contract Negotiator in Argentina or Mexico
hace 4 semanas
distrito federal, México IQVIA LLC A tiempo completoDevelop 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 Sponsor’s requirements.**Essential Functions** • Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text...
-
Clinical Trial Nurse Monterrey, Nuevo Leon, Mexico
hace 2 semanas
distrito federal, México IQVIA A tiempo completoClinical Trial Nurse Per Diem Work Set-Up: Local Travel In-Home Patient Visits Are you a Registered Nurse looking for a flexible and rewarding opportunity in clinical research. Join IQVIA, a global leader in advancing healthcare, and make a real impact by supporting clinical trials in your community. We’re seeking experienced Registered Nurses to visit...
-
Clinical Lead
hace 7 horas
distrito federal, México IQVIA A tiempo completoJob Overview The Clinical Lead provides leadership of the clinical team, in support of the project leader, and in collaboration with the other functional teams, to achieve the delivery of the project’s overall objectives to the Sponsor’s satisfaction per contract while optimizing speed, quality and cost of delivery and in accordance with our SOPs,...