Icon Clinical Research Work Values

Daily Duties at Icon Clinical Research:

Conducted all types of clinical monitoring visits (ie, pre-study, initiation, interim and closeout) which include all preparatory and follow up aspects. Monitored site performance and compliance and provide study team with updates and recommendations. Prepared clinical sites for regulatory agency audits. Assist sites and data management with query resolution. Developed subject recruitment strategies and collaborated with sites on meeting enrollment timelines. Mentor and co-monitor with junior CRAs. Assessed and reviewed subject medical records to ensure all serious adverse events/adverse events have been captured and documented in case report forms. Reviewed study documents to include protocol, case report forms, drug accountability and informed consents/processes.

What they like about Icon Clinical Research:

The social vibrance of a hiring firm is very important to you. Your ability to make and maintain friendships there is a critical part of your decision. You would likely be dissatisfied with a workplace that is quiet, cold, or otherwise not particularly social. When you investigate a new hiring company, ask recruiters, managers, and potential co-workers about the social life and opportunities there. This is especially important when you are relocating; moving dramatically alters your social sphere both inside and outside the workplace.

Tags

Clinical Research, Research, Medical, Medical Records, Monitoring, Documentation, Protocol, Complaints, Nursing, Ophthalmology

Skills

Clinical Research, Research, Medical, Monitoring, Documentation, Protocol, Nursing, Ophthalmology, Pharmaceuticals and Medical Devices, Oncology, Clinical Research, Cardiovascular, Leadership

These are some of the questions we asked our climbers about their experiences with Icon Clinical Research: