Paraxel International Work Values

Daily Duties at Paraxel International:

Perform remote clinical monitoring tasks and visits for designated projects in accordance with relevant SOPs and regulations ( prequalification, qualification, initiation, monitoring and termination) . Primary in-house site support, collaborating with CRA on site issues/actions . Perform regular reviews of data according to data review /monitoring guidelines ( EDMS, CTMS, CDMS/EDC, IVRS) . Communicate with trial sites on regular basis to ; review recruitment and enrollment updates, address protocol related questions . Check on site staff assignments, assess drug/study supply status, request outstanding trial related documents for the Trial Master Files. Address or resolve pending issues, follow-up on data entry, query status and SAEs and review site payment status .

What they like about Paraxel International:

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

Epidemiologist, Pharmacovigilance and Risk Management, Biostatistics, Health Service Research, Health Economics and Outcomes Research, Epidemiology, Data Analyst, SAS programming, Heath Scientist, Medicine, Public Health, Budgeting, Cost / Benefit Analysis, Presentations, Statistical Analysis, Pharmacoepidemiology, Consulting, Decision Analysis, Analytic Planning, Cost Accounting, SPSS, Active Program Monitoring, Stata, Training / Development, Workforce Planning, Longitudinal Data Analysis, Policy Development, Survival Analysis, Marginal Structural Models, Graphical Data Presentation, Needs Assessment, Public Relations, Project Management, Medical Terminology, Infectious Disease Epidemiology, Risk Management, Cohort / Case-Control Study Analysis, Proposal / Protocol Authorship, Prospective / Retrospective Studies, Drug / Vaccine Studies, Health Outcomes, Medical / Device Safety Surveillance, Disease / Body Systems, propensity scores, Standardization, Instrumental Variables, Signal Detection, Data Specification, Good Clinical Practice, GCP, Good Pharmacovigilance Practice, GPV, Safety Research, Study Design, Protocol Development, Electronic Data Capture, EDC, eTMF, TMF, Data Extraction, SAS Macros, Data Manipulation, Clinical Medical Monitor, Clinical Monitor, Principles of drug development, Drug development lifecycle, Safety Assessment

Skills

Advanced Epidemiological Methods, Data Analysis, SAS programming, SPSS and STATA, R programming, Clinical Research Methods, Clinical trial conduct and Trial Site Management, Clinical Project Management, Drug Development Process and Life Cycle Management, Medicine, Medical terminoogy, Medical Knowledge, Oral and written presentation skills, Scientific Writing, Good Clinical Practice, Team Work, including working in a virtual team, Trial Master Files

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