Pharmaresearch Corporation Work Values

Daily Duties at Pharmaresearch Corporation:

Monitored 9 sites and 2 protocols on a pivotal HIV clinical trial for Phase II and III in a salvage protocol, Audited a two year completed HIV clinical trial that was submitted to Bristol Myers Squibb and the FDA. Conducted drug accountability for studies and approved of hospital site destruction of investigational product per sponsor's SOP's. Performed initial, interim and closeout visits for assigned sites, Recruited investigators via internet search. Coordinated training at sites, Clarified and monitored case report form descrepancies, Notified sponsor of any protocol violations and instructed investigators of sponsor's corrections or exemptions, Collected additional serious adverse event report data while at site, Reviewed regulatory binder for completeness and verified all IRB documents present, Created newsletters for the study protocol. Created source document templates for the study.

What they like about Pharmaresearch Corporation:

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

pharmacovigilance, Sr. clinical research associate, Immunology, Oncology, Virology, Endocrinology, Cardiac markers, Data reconciliation, Clinical trials, Global delivery, Protocol development, Medical case management, Risk management, Clinical narratives, SAE reporting, Medical devices, IND queries, Regulatory reporting, Global unblinding, Safety database, Adverse event reporting, 21 CFR ICH, MedRa coding, WHO dictionary, IND reports, Regulatory submissions, Clinical study reports, Perodic Safety Update Reports PSUR, Quality auditing, Site Management, Monitoring, Teaching adults, Investigator meetings, Regulatory compliance, Internet recruiting, Drug development, Query resolution, Triage case workload, Oracle Argus II

Skills

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