In-depth knowledge of clinical trial conduct at clinical study sites for pharmaceutical research
Experience engaging with sites and key stakeholders throughout the lifecycle of a clinical trial.
Advanced Level of Portuguese
Advanced Level of Spanish
Advanced Level of English
Knowledge of patient recruitment practices and site-based processes and workflow.;
Possess knowledge and ability to apply ICH/GCP and applicable regulatory guidelines in delivery of services;.
Demonstrated ability to review and interpret data to identify trends and actions related to department delivery
Possess strong computer skills including proficiency in aspects of using remote technology and presentation software such as TEAMs, Microsoft Word, Excel, and PowerPoint.;
Excellent written and verbal communication, as well as presentation and training skills, including good command of English.;
Effective time management and organizational skills and ability to manage competing priorities.;
Strong attention to detail.;
Ability to adapt and be flexible in a global and dynamic work environment with changing priorities.;
Excellent interpersonal and problem-solving skills with ability to build and maintain strong relationships with IQVIA staff, site stakeholders, and other key stakeholders.;
Preferred: Experience in interviewing and selection of candidates for site assignments; Exposure and/or experience with site contracting process.
