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
Sr. Clinical Research Associate - São Paulo or Porto Alegre At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we
Study Start Up Associate II (Supporting North America region - US/CAN) At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships,
The Opportunity Executes day-to-day inventory & material management tasks at customer facilities, following a defined standard output or set of procedures. Tasks include receiving, inspection, inventory logging, proper storage, and timely distribution of inbound and outbound
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 than 750 biotechs,
Job Description Duration: 6 Months Contract To Hire Additional Job Description: Position works in groups that serve NCR’s small and medium sized customers. Position works in high call volume Helpdesk environment supporting NCRs customers in providing
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,