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 for a company with an emphasis on social values and helping society is a clear and important priority for you - a critical factor in who you choose to work for. In contrast to other factors, you place an organization's reputation for fairness and concern for the community above most other aspects of the company. As you search for a new job opportunity, it is usually possible to find out if the company is involved in the community and/or if it is addressing problems and issues in society. Pay special attention to non-profit organizations and those specifically involved in social action. Moreover, speaking with current and former employees should enlighten you to perceptions of the fairness of the company's leaders and the treatment of employees.

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: