Regulatory Submissions Jobs in Mexico

Sobre EYEY es una de las firmas de servicios profesionales más grandes del mundo dedicada a brindar servicios de auditoría impuestos asesoría y transacciones. Nuestro compromiso es construir un mejor mundo de trabajo ayudando a nuestros clientes a enfrentar sus desafíos más complejos y a aprovechar...

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications are made withi...

Regulatory & Start Up Specialist cFSP.Location: Mexico - Full home basedJob OverviewThis 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 suppo...

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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Regulatory Affairs Specialist 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 acro...

DescriptionIf you are an Import/Export Coordinator professional looking for an opportunity to grow your career: this role will give you the chance to coordinate the activities of the personnel responsible for import and export operations of raw materials and finished goods to optimize clearance time...

Sr. Associate I Regulatory Affairs Strategy Mexico City On-siteAt Alcon we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly champion progress and act with speed as the global leader in eye care. Here youll be recognized for your commitment and contributions...

About the RoleAs a Senior Site Navigator youll act as a local country or regional expert in studystart-up leading site-level activities with minimal oversight. Youll be a trusted partner tosites and internal teams proactively identifying risks mentoring junior colleagues andensuring studies move for...

Job LocationMEXICO CITY GENERAL OFFICEJob DescriptionWe are looking for the best talent in Interlomas General Offices to be:Regulatory Affairs InternPart-time positionStart date: 1st June 2026Location: Interlomas General OfficesWork schedule:part-time with flexible working hoursSalary:The gross sala...

Clinical Development CenterMexico CityAre you passionate about clinical trials and regulatory submissions Do you want to play a key role in ensuring high-quality execution of study start-up activities If so we are looking for a Start-Up Specialist to join our team and make a difference. Read more a...

Career CategoryRegulatoryJob DescriptionJoin Amgens Mission of Serving Patients At 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...

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...

Primary Function of PositionThe Sr. Regulatory Affairs Specialist Level 4 is an experienced professional responsible for leading strategic and operational regulatory activities across LATAM markets with primary focus on Mexico. This role ensures regulatory compliance manages product registrations an...

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-...

Regulatory & Start Up Specialist cFSP.Location: Mexico - Full home basedJob OverviewThis 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 suppo...

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight aga...

PurposeAs a Study Management Associate II 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 II works as a contributing member of a cross-functional and...

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...

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...

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...