and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical... monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues...
Lugar:
México | 22/02/2026 18:02:30 PM | Salario: S/. No Especificado | Empresa:
ICONWork Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Clinical... reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g...
or college, preferably in a job related major field of study - Minimum two (2) years of relevant professional experience... has a regular full time schedule with a normal work week of Monday through Friday. There may be a need for occasional work after...
. We are a global team of about 3,000 expert Consultants operating in Europe, North America, Asia, and Australia. We work... with senior stakeholders. Availability to travel frequently to Chihuahua. Experience with Procore or similar project management...
Pre Sales position is to work with the sales team, as its objective is to drive business development... meetings for sales presentations. Follow up on prospects and proposals. Create proposals and quotes. Work with the NA sales...
type: Full timeposted on: Posted Todayjob requisition id: JRApplyBoard simplifies the study abroad search, application... communication and collaboration with ApplyBoard teams.* Cross-Functional Collaboration: Work with internal teams to understand...
Study Support Assistant ICON plc is a world-leading healthcare intelligence and clinical research organization. We're... to shape the future of clinical development. We are looking for a Study Support Assistant for the Site Activation department...
Lugar:
Veracruz, Ver. | 22/02/2026 18:02:53 PM | Salario: S/. No Especificado | Empresa:
ICON management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols... of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP...
Lugar:
México | 22/02/2026 18:02:56 PM | Salario: S/. No Especificado | Empresa:
ICON - Travel within US, Mexico and other international locations as required. **Responsibilities and Authority**: - Support..., Operator Work Instruction, In-Process Inspection, Equipment Check Sheet, etc - Participates with multidisciplinary Team...
, and other ancillary agreements with study sites using critical thinking, available tools/systems/documents, historical data, and adheres... with ICON’s rules, procedures, and policies. Maintains consistent communication with study sites and internal stakeholders...