Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical
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 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
Medical Monitor Rheumatology, Canada or Argentina The Medical Monitor Rheumatology provides medical and scientific support to clinical research programs. The Medical Monitor will perform thorough data review to ensure data integrity and subject safety oversight, and
São Paulo, Brazil Mexico City, Mexico Buenos Aires, Argentina Santiago, Chile Lima, Peru Bogota, Colombia Full time R Job Overview A Central Monitor is a key skilled and clinically experienced team member of IQVIA Central Monitoring
Remote Clinical Trial Support Specialist (Multiple Openings) Company: Angel City VA — Virtual Clinical Research Support. Location: Remote (Philippines, Latin America,Georgia, Ukraine, Moldova, Armenia, Azerbajan) . Employment Type: Full-Time, Part-Time, and Project-Based Opportunities Available Join Angel
São Paulo, Brazil Mexico City, Mexico Buenos Aires, Argentina Santiago, Chile Lima, Peru Bogota, Colombia Full time R Job Overview An Assoc Central Monitor or Central Monitor is a key skilled and clinically experienced team member
São Paulo, Brazil Buenos Aires, Argentina Full time R JOB SUMMARY: Responsible for medical data review and medical safety case processing and related safety activities. Performs review of medical data to ensure medical/scientific plausibility and to
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