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The Medical team is looking for an Associate Medical Director specialized in Psychiatry. Job Overview Primarily acts as global and regional Medical Advisor but may serve as back-up Medical Advisor on assigned projects. Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications,...

Buenos Aires ThermoFisher Scientific Ayer Work Schedule Standard (Mon-Fri) Environmental Conditions Office 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 750 biotechs, spanning 2,700 clinical trials across 100+...

Job Overview The Associate Medical Director / Medical Director - Dermatology will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested; participate in all aspects of Medical Science involvement on assigned trials; serve as a medical expert during project delivery lifecycle; provide therapeutic and medical expertise...

Senior Medical Director, Hematology/OncologyBuenos Aires, ArgentinaMexico City, MexicoSão Paulo, BrazilFull timeRJob OverviewThe Senior Medical Director (Hematology/Oncology) is a strategic medical leader who provides scientific, clinical, and operational oversight across global clinical research programs. Acting as Medical Monitor, this role serves as the...

Job Overview The Associate Medical Director / Medical Director - Dermatology will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested; participate in all aspects of Medical Science involvement on assigned trials; serve as a medical expert during project delivery lifecycle; provide therapeutic and medical expertise...

Job Overview A Central Monitor is a key skilled and clinically experienced team member of IQVIA Central Monitoring Department. Provides remote project support and assistance across multiple projects, sites and teams and reviews the structured clinical data output with access to medical charts. Essential Functions: Perform centralized monitoring activities...

The Medical team is looking for an Associate Medical Director specialized in Psychiatry.Job Overview Primarily acts as global and regional Medical Advisor but may serve as back-up Medical Advisor on assigned projects. Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications,...

Job Overview A Central Monitor is a key skilled and clinically experienced team member of IQVIA Central Monitoring Department. Provides remote project support and assistance across multiple projects, sites and teams and reviews the structured clinical data output with access to medical charts. A Central Monitor is a key skilled and clinically experienced...

Senior Medical Director, Hematology/OncologyBuenos Aires, ArgentinaMexico City, MexicoSão Paulo, BrazilFull timeRJob Posting Title- Senior Medical Director, Hematology/OncologyLocation: Home-based in the U.S. or CanadaJob OverviewThe Senior Medical Director (Hematology/Oncology) is a strategic medical leader who provides scientific, clinical, and...

Job OverviewThe Associate Medical Director / Medical Director - Dermatology will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested; participate in all aspects of Medical Science involvement on assigned trials; serve as a medical expert during project delivery lifecycle; provide therapeutic and medical expertise...

Job Posting Title- Senior Medical Director, Hematology/OncologyLocation: Home-based in the U.S. or CanadaJob OverviewThe Senior Medical Director (Hematology/Oncology) is a strategic medical leader who provides scientific, clinical, and operational oversight across global clinical research programs. Acting as Medical Monitor, this role serves as the primary...

Job Overview The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans, as assigned. Function as leader for projects of limited scope, as assigned....

Work Schedule Standard (Mon-Fri) Environmental Conditions Office 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 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As...

Parexel FSP is looking for CRAs to join our team in Argentina. We are looking for candidates with +1 year of monitoring experience, based in Buenos Aires. The Clinical Research Associate will be responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line with...

Job OverviewSite monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.ResponsibilitiesResponsible for all aspects of study site monitoring including routine monitoring and closeout of clinical...

Buenos Aires ThermoFisher ScientificHoyWork ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as an Assistant Clinical Research Associate - Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+...

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.Summary of Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring and closeout...

Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or...

Job OverviewSite monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of study site monitoring including routine monitoring and...