Regulatory Documents Jobs in Mexico
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Operations Legal And Compliance Repse Specialist
Ge Vernova
Job Description SummaryLawyers and non-lawyers providing leadership and oversight to business operations to assure adherence to all aspects of internal company and external regulatory compliance. Insures appropriate mechanisms are in place to comply with relevant laws and regulations and adherence t...
Latam Gcs Sr Project Coordinator
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of our PPD clinical research team youll have the opportunity to support groundbreaking studies that make a real difference in patients lives.Position SummaryAs Senior Project Coordinator you will provide administrati...
Clinical Trial Coord
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Coordinator Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 cou...
Regulatory Solutions Reports & Demands
Nubank
About UsNu is one of the largest digital financial platforms in the world with more than 127 million customers across Brazil Mexico and Colombia. Guided by our mission to fight complexity and empower people we are redefining financial services in Latin America and this is still just the beginning of...
Regulatory Solutions Reports & Demands
Us Nu
About UsNu is one of the largest digital financial platforms in the world with more than 127 million customers across Brazil Mexico and Colombia. Guided by our mission to fight complexity and empower people we are redefining financial services in Latin America and this is still just the beginning of...
Reg & Start Up Specialist I
Iqvia
Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenance activities.Es...
Trial Delivery Specialist Clinical Trial Coordinat...
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Coordinator Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 cou...
Medical Director Senior Medical Director Hematolog...
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionSummarized Purpose: Provides medical oversight of clinical trials to ensure company SOPs client directives good clinical practice and regulatory requirements are followed. Attends and presents at investigator and sponsor mee...
Clin Ops Delivery Associate (ctc)
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Clinical Trial Coordinator Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across...
Regulatory Affairs Analyst
Johnson & Johnson
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...
Clinical Study Administrator
Astrazeneca
The Clinical Study Administrator (CSA) assists in the coordination and administration of the study activities from the start up to execution and close out and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time cost and quality objectives....
Cra Ii
Fortrea
Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...
Clinical Trials Lead Site Coordinator
Psi Cro
Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP protocol requirements within Study specific defined timelines and enrollment goals.In this role you will:Act as the main line of communication between the Sponsor or CRO and the site.Ensure response to...
Regulatory & Quality Documentation Specialist
P3 Usa
The unique aspect of our business is the mindset of our employees: curious adventurous and innovative. P3 consultants take on early responsibilities with clients in management consulting diverse technology topics and scalable IT solutions.Make a project your project. Openness for new innovative and...
Clinical Research Associate
Psi Cro
Only CVs in English will be consideredWe are looking for a CRA to join our team in Mexico. Here you will have the opportunity to develop yourself as a senior trainer mentor and leader. We are committed to develop our employees in their careers by providing tailored courses and mentoring.Responsibili...
Sr. Associate Law (cdmx)
Amgen
Career CategoryLaw/LegalJob DescriptionJoin Amgens Mission of Serving PatientsAt Amgen if you feel like youre part of something bigger its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.Since 1980 weve helped pioneer the world of biotech in ou...
Regulatory Senior Associate Chemistry, Manufacturi...
Pfizer
Work Location Assignment:Mexico City must be able to work from assigned Pfizer office 2-3 days per week or as needed by the businessUse Your Power for PurposeAt Pfizer we are committed to bringing medicines to the world with speed without compromising on excellence and integrity. Navigating the ever...
Clinical Trial Coordinator I-ii
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Clinical Trial Coordinator Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across...
Principal Reg Affairs Spec
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionIn this role you will be a pivotal team member withregulatory affairs responsibilities leading discussions and coordinating regulatory strategies globally on assigned (Phase 1 to 4) clinical trials studies and projects.You w...
Principal Ra Sepcialist
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionIn this role you will be a pivotal team member withregulatory affairs responsibilities leading discussions and coordinating regulatory strategies globally on assigned (Phase 1 to 4) clinical trials studies and projects.You w...