Covance Inc. Work Values

Daily Duties at Covance Inc.:

• Conducted all aspects of site monitoring including qualification, initiation, active-phase, and termination visits in accordance with GCPs and global SOPs to assess the safety and efficacy of investigational products. • Conducted site visits, monitored Case Report Forms and on-site source documentation, performed study drug accountability, assisted site Study Coordinators with completion and source-verification of Data Clarification Forms, met with Principle Investigators to discuss the progress of the study. • Prepared sites for regulatory inspections, conducted training and remedial training for non-compliant sites. • Experienced with IVRS systems, single-blind, double-blind, and open-label clinical trials. • Managed the INDSR reporting process, including submission to the Central IRB on behalf of sites and resolution of site-specific INDSR discrepancies. • Assisted the client with resolution of outstanding SAE reports and SAE follow-up on a site-specific level.

What they like about Covance Inc.:

Organizations with strong, centralized leadership are particularly attractive to you. You require a work environment with leadership that aggressively seeks to expand and grow the business and does so in a visible and decisive manner. In general you prefer to work in an environment in which there is a strong link between leadership, its actions, and a strong set of company-wide values.

Tags

CCRA, Florida, southeast, oncology, manager, IMPACT, RAVE, Phase I, Phase II, Phase III, CTMS, audit, CRA, clinical, research, associate, senior, experienced, management

Skills

Clinical Trial Management, Audit Response, Clinical Trial Management Systems, Electronic Data Capture, Contracts and Budgets - Creation and Management, Monitoring, Pharmacokinetics and Pharmacogentics, Investigator Payments - Schedule and Management, Data Lock Timelines, Recruitment Plans and Contingencies, Monitoring Plan Development and Execution, Corrective and Preventive Action Plan(s) - CAPA(s), Blinded Trial Management, Oral and IV Drug Accountability, Informed Consent Development

These are some of the questions we asked our climbers about their experiences with Covance Inc.: