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:

You give high priority to hiring firms with prestige. Market reputation and prestige of a firm may be determined through on-line research, and conversations with individuals working in your target industry. Note that firms "in the public eye" receive a great deal more critical publicity and attention than those operating with more anonymity. So as you assess your employment opportunities, be sure to seek out the positive aspects of the firm's reputation in addition to noting negative publicity the company may have received.

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: