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Skills
Biometricsunmatched
Biostatisticsunmatched
Clinical Researchunmatched
Contract Research Organization (CRO)unmatched
Data Managementunmatched
Detail Orientedunmatched
GCP (Good Clinical Practices)unmatched
GMP (Good Manufacturing Practices)unmatched
Information Technology & Information Systemsunmatched
Leadershipunmatched
Magnetic Resonance Imaging (MRI)unmatched
Maintain Complianceunmatched
Project/Program Managementunmatched
Quality Managementunmatched
Regulationsunmatched
Rehabilitation Nursingunmatched
Standard Operating Procedures (SOP)unmatched
Statistical Analysis System (SAS)unmatched
Statistical Programming Languagesunmatched
Vendor/Supplier Evaluationunmatched
Description
Statistical Programmer (SAS Programmer)Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionJob Title: Sr. Associate, Biometrics QualityLocation: Cambridge, MADuration: 12+ months (possibility of extension)Roles & Responsibilities:The Biometrics Quality Team provides leadership and support for the Global Biometrics department, which consists of Data Management, Biostatistics and Statistical Programming.The Sr. Associate, Biometrics Quality role will be responsible for:Conducting reviews to ensure compliance with SOPs and other documents.Leading capability assessments of Biometrics vendors including CROs and 3rd Party Vendors (ePRO, MRI, etc).Providing support to Biometrics staff with quality activities including CAPAs and process deviations.Support for Inspection Readiness and Regulatory InspectionsRequired:7+ years relevant work experience in Data Management, Biostatistics or Statistical Programming.7+ years relevant work experience in GCP Quality with significant interaction with Data Management, Biostatistics or Statistical Programming.Knowledge of GCP and other regulations.Experience with Quality Issue Management (e.g. CAPAs) and/or Regulatory Inspections.Strong project management skills; high attention to detail with proven ability to manage multiple, competing priorities;Ability to work effectively across functions and levelsPlease note this is not a GMP Quality role