Regulatory Submissions Jobs in Mexico
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Regulatory Submissions Associate Manager Ii Apac
Fortrea
Job Overview:In the role you will collaborate with key stakeholders across the organization and at times be client facing to achieve client-centric delivery in a matrix organization. Oversight and accountability of Regulatory Authority (RA) Independent Review Board (IRB)/Ethics Committee (EC) and Th...
Sr Cra 1 Or Cra 2
Iqvia
Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Essential Functions Perform site monitoring visits (selection initiatio...
Site Navigator Ii
Fortrea
Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites this role ensures...
Study Start Up Lead
Roche
At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...
Associate Dir, Qara Mx N. Cluster
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...
Regulatory Affairs Manager Camex
Beiersdorf
At Beiersdorf we want to help people feel good about their skin and our commitment goes far beyond caring for skin. For 140 years we have developed innovative skin and body care products for well-known brands such as NIVEA Eucerin La Prairie Hansaplast and Labello. We act according to our purpose W...
Clinical Team Manager (ctm) – Hemonc
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Manager - Make an Impact at the Forefront of InnovationThe Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specifi...
Study Management Associate Iii
Abbvie
PurposeAs a Study Management Associate III you will be part of a dynamic centralized study management team that is responsible for the execution of our global clinical trials and a key member of the study team.The Study Management Associate III works as an independent contributing member of a cross-...
Risk Management Engineer 3
Intuitive
Primary Function of PositionAs Intuitives da Vinci Surgical System and other medical devices become adopted by an increasing population of hospitals surgeons and patients we are building a focused team to drive reliability quality and safety to ever-better levels. This focus applies to product in us...
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...
Analyst Regulatory Affairs Fixed Term 12 Months
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...
Sr. Icf Project Manager
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Medical Writer - Make an Impact at the Forefront of InnovationThe Senior Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts...
Country Approval Specialist
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Country Approval Specialist for North America assignations Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 270...
Tax Compliance Officer 18350 Cg
Somewhere
Job Title: Tax Compliance OfficerSalary: $1000-$2000Remote full-timeLocation: LATAM (Mexico preferred)OverviewWe are seeking a detail-oriented and highly organized Tax Compliance Officer to ensure accurate tax reporting regulatory compliance and financial record management. This role requires strong...
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...
Coordinating Cra
Iqvia
External Job DescriptionJob OverviewPerform monitoring and site management work for a variety of protocols site and therapeutic areas.Essential Functions Perform site monitoring visits (selection initiation monitoring and close-out visits) in accordance with contracted scope of work and regulatory r...
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...