Manager, Regulatory & Start Up – Sponsor Dedicated 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, oversight of the scope of
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Data Team Lead – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Clinical Vendor Oversight Specialist Make an impact. Advance science. Grow your career. At Thermo Fisher Scientific, youll be part of a global team committed to making the world healthier,
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Get started on an exciting career at Element! Element employees make a difference in the lives of others every day. We are re-defining the fleet management industry to be people first, then business – delivering on
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than
Job Summary The Study Manager is part of the ( DMTI - Digital Medicine and Translational Imaging ) group, that looks to develop and implement novel technologies to support companys portfolio studies. In particular for this
Job Summary The Clinical Scientist (CS) will provide of observational study execution including epidemiological, non-interventional, pragmatic and low-interventional studies and research collaborations to ensure consistency of approach, conduct, monitoring, analysis, reporting, and oversight of core team
Home Based - México ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion
Primary Location : Mexico, Remote Job ID R Category Medical Sciences ABOUT THIS ROLE : Job Summary - Accountableforallcountryclinical/medicalaspectsassociatedwithDevelopmentandprioritizedRe-search programs/trialsbyprovidingclinicalstrategicandtacticalleadershipastheCountryClinicalDevelopment representative. May work across several countries. - Gathers,informs,andactsonclinical/medical/scientificinsightsforclinicaltrialconceptsheets/protocols, InformedConsentForms(ICFs)andotherrelevantclinicaldocumentstooptimizeclinicaltrialimplementation. - Drivestheidentificationandinvolvementofqualifiedinvestigatorswithgreatestrecruitmentpotential,identifies clinicalrecruitmenthurdlesanddrivesclinicalrecruitmentactivitiestoovercomethesehurdles. - Accountableforadherencetosafetystandardsandclinicaldataqualityinthecountrybyprovidinggeneral clinical/medicalsupportfortrialrelatedsafetyfindings. -
Provides study level operational support to the Core Study Team from study start up to close out and submission with general direction: - Management and oversight of Study Team shared spaces - TMF maintenance, compliance, and
At Thermo Fisher Scientific, you’ll 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
Site Activation Specialist for External Commerce (ComEx) - Homebased Essential Functions - Responsible for importations and exportation activities in Mexico for our FSP model - Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of
Parexel FSP is hiring multiple Site Care Partners in Mexico! Excellent opportunity for experienced Senior CRAs ready to take the next step in their career! The Site Care Partner (SCP) is the face of the client and
Qualifications : Education and Experience: Bachelors degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 5 years). 1+
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Purpose : - Clinical Trial Coordinator - Project Specialist is a key member of the Global Study Team contributing to delivering the clinical study to time, cost and