Clinical Data Analyst

Job Category: Biotech/R&D/Science Career Level: Experienced (Non-Manager) Location: Baltimore, MD 21225           Job Description: PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, medical marketing and consulting services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Headquartered near Boston, Massachusetts, PAREXEL operates in 55 locations throughout 43 countries around the world, and has over 6,315 employees. For more information about PAREXEL International visit www.PAREXEL.com Job Title Clinical Data AnalystDepartment Biometrics & Data ServicesSBU Clinical PharmacologyLocation Baltimore, MDEssential Function Responsible for the conduct and execution of data management plans for the design, and implementation of clinical data collection, review, and reporting systems for clinical studies. Ensures standardized database structures, naming conventions, codelist, are adhered to. Supports project Biostatisticians in the generation of tables, listings, and figures to be included in clinical summary reports using SAS.RelationshipsReports To Director, Biometrics & Data ServicesDirectly Supervises noneProvides Work Direction to noneWorks Closely with All departmental membersExternal Relationships noneKey Accountabilities' Design, test, implement, and document clinical trial databases. ' QC database structure, naming conventions, and codelist to ensure standardization and clinical trial requirements are met.' Review Case Report Forms (CRFs) to ensure consistency with protocol and adequacy in collecting data to meet objectives defined in protocol ' Writes and QC validation programs according to specifications.' Modifies and cleans external electronic data according to specifications.' Perform analysis of clinical data per defined requirements.' Support biostatistics and reporting by producing summary tables, patient data listings, and figures, for clinical studies using SAS according to the sponsor formatting specifications or as documented in the Statistical Analysis Plan.' Debug, troubleshoot, and review SAS programs.' Participate in SOP development.' Other responsibilities as assigned by immediate supervisor. Skills ' Strong analytical skills.' Ability to effectively apply technical knowledge to solve problems.' Self motivated, able to independently, demonstrates a functional understanding of clinical trial database design and a basic knowledge of SAS.Education' BS/MS in health related science or equivalent experience.' Some statistical training preferred.Language Skills' EnglishMinimum Work Experience' At least 2-5 years clinical and/or research experience preferred RESPOND HERE! Respond immediately by accessing the following dedicated online response form which will allow you to cut and paste your resume. This form will go directly and immediately to the hiring authority for this position. Access the online response form at: http://sh.webhire.com/servlet/resp/rf?jobid=2237819&boardid=749