Noguchi Memorial Institute Of Medical Research Work Values

Daily Duties at Noguchi Memorial Institute Of Medical Research:

Sub-investigator for an NIH/NIAID funded project to build capacity and prepare sites in West Africa to conduct clinical trials. Designing, conducting and analyzing studies that required data collection, including direct collection from patients and healthcare providers, and chart review. As well as analyzing data that require secondary databases. Responsibilities included: Subject matter expert drug and vaccine studies, provide scientific direction and guide project execution in collaboration with other team members Study design and protocol development to meet both local and external regulatory requirements, designing data collection forms - Case Report Forms, Informed Consent Forms. Study site selection and preparation; determining the material and human resources needed per protocol, contributing to multiple projects and studies concurrently. Coordinating communication and submissions between investigating site and multiple Institutional Review Boards, Regulatory Authorities and collaborating Investigators. Direct client contact and contributing to study budget preparation. Writing Standard Operating Procedures and Study Specific Procedures. Preparation of abstracts, manuscripts and oral presentations, including development of slides and posters for presentation of project results at meetings Clinical trial activities including: Recruitment and screening of study subjects, following eligibility criteria of the protocol. Completing source documents and Case Report Forms Patient Safety Surveillance / Assessment and reporting of Adverse Events As a member of quality management team, I was responsible for ensuring quality compliance by the clinical and immunology laboratories. Tracking maintenance of clinical equipment and non-investigational drugs. Investigational drug receipt and accountability Training of other support staff in good clinical practice guidelines, good clinical laboratory practice and protocol specific procedures. Served as internal reviewer and mentor to research associates and technical staff in the clinical laboratory.

What they like about Noguchi Memorial Institute Of Medical Research:

A hiring company that offers alternative approaches to pay, performance bonuses, and/or equity in the firm is very attractive to you. You're generally less interested in working for an organization offering only traditional, salary-based compensation, one with limited opportunity to acquire equity in the firm, or one that does not actively promote skill development. In addition, you are more likely to choose a company that offers a variety of internal career options, with defined career paths. You view the learning of new skills and development of your expertise as key to your career advancement. These aspects of an organization may become even more important to you as you progress in your field, and are especially critical if you change career or occupation.

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 Noguchi Memorial Institute Of Medical Research: