statistical programmer(SAS Programmer)
IntegratedResourcesINC
Posted: May 12, 2016
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Quick Summary
We are seeking a Sr. Associate, Biometrics Quality to join our team in Cambridge, MA. The ideal candidate will have experience in biometrics and quality assurance, with a strong understanding of statistical programming languages such as SAS. The successful candidate will be responsible for ensuring the quality of biometric data and providing technical support to our clients.
Required Skills
Job Description
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 Title: Sr. Associate, Biometrics Quality
Location: Cambridge, MA
Duration: 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 Inspections
Required
• 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 levels
Please note this is not a GMP Quality role
Thanks & Regards,
Seema Chawhan
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
DIRECT # - 732 – 318 -6506 | (W) # 732-549-2030 – Ext – 324 | (F) 732-549-5549
Email id – seema @irionline.com| www.irionline.com
LinkedIn: https://in.linkedin.com/in/seemachawhan
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