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Product data entry analyst/ sample handling support

Integrated Resources, Inc

Chesterfield, Missouri

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JOB DETAILS
JOB TYPE
Contractor
SKILLS
Analysis Skills, Antibodies, Biochemistry, Biology, Chemistry, Clinical Research, Computer Skills, Data Analysis, Data Entry, Drug Development, GCP (Good Clinical Practices), GMP (Good Manufacturing Practices), Information Technology & Information Systems, Laboratory Information Management System (LIMS), Microsoft Excel, Microsoft Office, Microsoft Word, Regulatory Submissions, Rehabilitation Nursing, Sample/Specimen Processing
LOCATION
Chesterfield, Missouri
POSTED
1 day ago
Product Data Entry Analyst/ Sample Handling SupportA Few Words About Us 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 DescriptionOur client is looking for Product data entry analyst/ sample handling support- with good Clinical Practices, Data entry, LIMS, GMP, Data transcription / verification, and LIMS sample review experience etc.RESPONSIBILITIES:Data transcription, review, and trending of biologics (mAb, antibody drug conjugate, etc) stability data in preparation for regulatory filings.Specifically, the analyst will be expected to: Retrieve data from LIMS (Laboratory Information Management System) database or other data repository.Transcribe data into stability sections of regulatory filings, or perform 100% accuracy verification for previously transcribed data; Review sample results within LIMS to identify incomplete testingNotify Stability Lead of any unusual findings or gaps in data; Assist Stability Leads with various tasks as necessaryAssist with sample handling duties as needed (shipment receipt, aliquoting, etc.)QualificationsQUALIFICATIONS AND SKILLS NEEDED:• Background in biochemistry, biology, chemistry, or related scientific discipline; Understanding of normal pharmaceutical development processes• Ability to work in a highly regulated environment and learn/comply with GMP expectations; Ability to accurately transcribe data from Excel documents to MS Word; Ability to thrive in a fast-paced environment and adapt to changing priorities; Familiar with Microsoft Office Suite, and computer literate enough to quickly learn new systems.

About the Company

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Integrated Resources, Inc