Principal Biostatistician @ EMD Serono, Inc. / Merck Serono
Biostatistician @ Dana-Farber Cancer Institute
Graduate Research Assistant @ Rho
Education:
Bachelor of Science @
Clemson University
About:
Over 7 years experience in medical research, specifically in cancer and quality of life. Skilled in international and interpersonal collaboration, project management, SAS programming, statistical analysis, and public speaking.
Specialties
Analysis Planning, Statistical Analysis, Manuscript Preparation, Grant Writing, Protocol Development and Design, Project Management, Presenting International, Local, and Web-based Trainings, Data Cleaning, Trouble Shooting, Treatment Monitoring, and
Over 7 years experience in medical research, specifically in cancer and quality of life. Skilled in international and interpersonal collaboration, project management, SAS programming, statistical analysis, and public speaking.
Specialties
Analysis Planning, Statistical Analysis, Manuscript Preparation, Grant Writing, Protocol Development and Design, Project Management, Presenting International, Local, and Web-based Trainings, Data Cleaning, Trouble Shooting, Treatment Monitoring, and Statistical Programming.
Principal Biostatistician @ From June 2013 to Present (2 years 5 months) Greater Boston AreaBiostatistician @ • International Breast Cancer Group (IBCSG) Trial Statistician for large Phase III Trial (4000+ patients) and Quality of Life (QL) Statistician for all IBCSG Trials (Phase II-III). Prepare Statistical Analysis Plans, Treatment Monitoring and Data Submission Reports, Biostatistician’s Reports, DSMC Reports, FDA reports.
• Dana-Farber/Harvard Cancer Center (DF/HCC) Non-Melanoma, Skin Cancer Statistician and lead statistician on select QL and nurse-initiated studies at DF/HCC. Statistician for Hematopoietic Stem Cell Transplantation (HSCT) under the direction of a Senior Statistician (2008 – 2011).
• Provide statistical support to investigators for grant preparation and submission. Collaborate with investigators and statisticians on study design, and CRF and protocol development. Responsible for analysis planning (Phases I – III; exploratory; retrospective). Prepare and review abstracts, posters, presentations, and manuscripts for submission. Monitor eligibility of patients, queries, compliance, and consistency of data. Train incoming statisticians and data managers as requested. From July 2008 to June 2013 (5 years) Greater Boston AreaGraduate Research Assistant @ • Created a Statistical Analysis Plan (SAP) for a client under the supervision of Senior Biostatisticians and University of North Carolina Adjunct Faculty.
• Prepared specifications for analysis datasets, summary tables, summary listings, and graphical displays for proposed research protocols.
• Assisted with the preparation of Statistical Analysis Plans and Statistical Reports for client projects.
• Validated analysis datasets, tables, listings, and figures using specifications and SAS programming.
• Created graphical data displays for client projects.
• Identified and troubleshot missing, miscoded, and incomplete data. From August 2006 to June 2008 (1 year 11 months) Durham, NC
Masters of Science, Biostatistics @ University of North Carolina at Chapel Hill From 2006 to 2008 Bachelor of Science, Mathematical Sciences with Emphasis in Statistics @ Clemson University From 2002 to 2006 Curtin UniversityHeathwood Julie Aldridge is skilled in: Biostatistics, SAS programming, Statistics, Data Management, Statistical Analysis..., Statistical Data..., Oncology, Patient Reported..., HRQOL (Health Related..., Survival Analysis, Competing Risks, Public Speaking, Photoshop, Illustrator, Clinical Study Design
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Worked briefly for Layer3tv/T-mobile as a contract employee, now have a full-time position with Oracle working on enhancements for cloud storage customers.