Clinical Trials Jobs in Mexico
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Latam Regulatory Affairs Senior Team Manager Cdmx
Mars
Job Description:The LATAM Regulatory Affairs Senior Team Manager leads the Regulatory Team and works collaboratively with cross-functional partners (included but not limited to the VCO Sales and Marketing teams and Corporate Affairs Directors) to support the companys LATAM regional and global object...
Regional Medical Affairs Manager Sr Regional Medic...
Gossamer Bio
Summary:The Regional Medical Affairs Manager / Sr Regional Medical Affairs Manager will be responsible for facilitating scientific exchange and clinical support for Gossamers clinical studies and will engage with clinical study sites investigators and study personnel to encourage fast study start up...
Sr Proj Mgr Clin Supplies
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and...
Oncology Medical Director
Msd
Job DescriptionRole summary:The Mexico Therapeutic Area lead (TAL) is a role within value and Implementation Global Medical and Scientific Affairs (V&I GMSA) reporting directly to the Mexico Medical Director (CMD) and is an important medical leader and point of contact for the therapeutic area (TA)-...
Vaccines Pharma Medical Director
Msd
Job DescriptionRole summaryThe Therapeutic Area lead is a role within Value and Implementation Global Medical and Scientific Affairs reporting directly to the Executive Country Medical Director and is an important medical leader and point of contact for the therapeutic area -related activities for M...
(sr) Clinical Project Manager - Talent Pool
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and...
Fsp Contract Negotiator In Mexico
Iqvia
Support the delivery of all required start-up contracting activities for selected sponsors studies or multi-protocol programs as determined by either the agreed algorithm or the Sponsors requirements including pre-award activities.Essential Functions Develop simple investigator grant estimates and p...
Fsp - Contract Negotiator In Mexico
Msc Quintiles Mexico S. De R.l.
Support the delivery of all required start-up contracting activities for selected sponsors studies or multi-protocol programs as determined by either the agreed algorithm or the Sponsors requirements including pre-award activities.Essential Functions Develop simple investigator grant estimates and p...
Director, Product - Clinical Study Monitoring
Fortrea
Job Overview:The Director of Product Management serving as the Product Owner of a domain or platform of products will lead the strategy and development of our life sciences software with a focus on our Clinical Platform. This role is pivotal in crafting innovative solutions that meet the evolving ne...
Site Readiness And Reg Specialist Ii
Fortrea
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...
Start-up & Regulatory Specialist Ii
Fortrea
Shape the Future of Global Clinical TrialsJoin our dynamic team and lead the crucial start-up phase of impactful clinical trials with opportunities for international exposure. Youll ensure projects are delivered on time within budget and to the highest quality standards directly contributing to life...
Core Icf Developer/writer And Reviewer (centralize...
Fortrea
Tasks:Responsible for developing reviewing finalizing and maintaining clinical trial documents such as informed consent forms. Applies knowledge of GCP Guidelines regulatory requirements regulatory framework of privacy standards and biological samples standards therapeutic area(s) and Investigationa...
Clinical Trial Coordinator- Fsp
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionCTC Functional Service Partnership Job Purpose: Clinical Trial Coordinator Project Specialist is a key member of the Global Study Team giving to delivering the clinical study to time cost and quality and ensuring inspectio...
Data Operations Real Assets Data Manager
Msci
Your Team ResponsibilitiesWe are seeking an experienced and detail-oriented Senior Associate to join our Real Estate Data Quality Team. This role will focus on ensuring the accuracy completeness and reliability of real estate data within our systems supporting decision-making compliance and reportin...
Medical Science Liaison
Iqvia™
IQVIA is The Human Data Science Company focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles IQVIA offers a broad range of solutions that harness advances in healthcare information technology anal...