Unlimited. Work Remote. The Role As a Protocol Review Specialist, you\'ll conduct 20-minute consultative appointments.... Our Protocol Review Specialists enjoy a calendar full of scheduled appointments, a beautifully designed and fast CRM and Phone...
Protocol Review Specialist We create best-in-class products – from anti-aging serums, to immune support formulas.... Earn Unlimited. Work Remote. As a Protocol Review Specialist, you'll conduct 20-minute consultative appointments...
Protocol Review Specialist We create best-in-class products – from anti-aging serums, to immune support formulas.... Earn Unlimited. Work Remote. As a Protocol Review Specialist, you'll conduct 20-minute consultative appointments...
Specialist assigned to Client in MEX or ARG with Clinical Trials experience Syneos Health® is a leading fully integrated...-specific contracts from country template. Submits proposed CTA and investigator budget for site review. Negotiates budget...
and supervision of a line manager or delegate, liaises with internal stakeholders to review sponsor requirements, protocol...Global Feasibility Specialist Home Based Argentina Description Global Feasibility Specialist Home Based Argentina...
Global Feasibility Specialist Home Based Argentina Description Global Feasibility Specialist Home Based Argentina... activities. Under guidance and supervision of a line manager or delegate, liaises with internal stakeholders to review sponsor...
to review sponsor requirements, protocol, and timelines for individual RFPs. Limited and guided research of scientific...Updated: Yesterday Location: Buenos Aires, B, Argentina Job ID: 25103343 Description Global Feasibility Specialist...
team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing... protocol compliance, data integrity, and patient safety throughout the trial process. - Collaborating with investigators...
and practices. Provide project-related support across multiple projects, sites and teams and review the structured clinical data...) and applicable regulatory requirements. Adherence to protocol, overall completeness, and readiness of the supplied patient...
team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing... protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators...