Valeritas Work Values

Daily Duties at Valeritas:

● Clinical study site monitoring through travel to clinical sites for review of protocol compliance, individual subject source documents and data collected (source data verification), clinical site regulatory and other documentation compliance accordingly. ● Enforces and ensures adherence to GCPs of all clinical sites, applicable regulations and internal quality system requirements. ● Monitors clinical sites for quality management as well as workload management. ● Solve problems encountered at clinical sites or internally during a study. ● Travel locally and within the US.

What they like about Valeritas:

Working in an organization that is technologically advanced, creative, and innovative is critical in your assessment of hiring companies. Less important to you are stability of the organization, the length of time an organization has been in business, and the business' plans for the future. You prefer a fast-moving company that will take risks to achieve its goals and objectives. The length of time the company has been in business is irrelevant. Maintaining status quo is unnecessary. You thrive on change, uncertainty and the upside of potential business risks, especially those associated with innovation. Stability for the long haul is not nearly as important as is working in an atmosphere that is charged with a sense of urgency and constant change.

Tags

CRA, Site Monitor, Study Manager, Trial, Clinical Trial, Drug Safety, Pharmacoviligence, Medical Device, Quality Assurance, Quality Control, Regulatory, Research, Clinical Research, Medical Sales, Associate Scientist, biopharmaceutical, biothechnology, clinical researh associate, protocol, coordinator

Skills

PowerPoint , Microsoft Office, Direct Site Monitoring, Regulatory Document Review, Phase II - IV Clinical Trials, EDC

These are some of the questions we asked our climbers about their experiences with Valeritas: