Parexel International Work Values

Daily Duties at Parexel International:

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 Parexel International:

You highly value a work environment built on a formal structure, rules, and regulations. You do not enjoy the unpredictability of shifting priorities and deadlines that upset your routine. You require and enjoy direction, input and accountability as part of your work environment. You have a strong need to participate in making key decisions and feel left out if your superiors or co-workers do not seek your input when making decisions. You thrive on providing good customer service to both internal or external customers, and doing so makes you feel good.

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 Parexel International: