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Responsible for independently coordinating all activities associated with timely packaging, labeling and assembly of clinical materials for designated domestic and international studies ...
Shift: Day 7am-7pm - Night 7pm-7am switch every 3 months. Rotate 3/2 days with every other weekend. During the initial training (3 weeks) will be 7am-3pm Mon-Fri schedule.Job Description The ...
Job description/Principal Responsibilities: Design and carry out bench scale fermentation process under guidance of scientist. Perform enzymatic and analytical assays, analyze data, and ...
Monday through Friday - Standard Daytime Hours Will work primarily with water based chemicals. Work with Research Scientists to test polymers for the construction market Complete laboratory ...
Chemistry laboratory technicians assist chemists in their lab work. As time progresses, lab technicians are completing a greater number of tasks that previously would have been performed by highly ...
Schedule: We have created a facility for high throughput screening for COVID-19 of our Key Workers. Staff within this laboratory will work a shift pattern to enable a 16-hour day operation ...
Commitment of a 40-hour work week in West Greenwich, RIQuality Control Bioanalytics is searching is for an analytical scientist to support testing for product routine and stability samples for ...
Job Purpose: Under daily supervision, supports the aseptic set up, sanitization, manufacture (compounding, fill) and finishing (label, bulk shipment) of sterile clinical products according to cGMP ...
The Periodic Reporting Project Manager will be expected to prepare and review Medicare Secondary Payer (MSP) Reports. Medicare Secondary Payer is a federally mandated report, submitted quarterly to ...
Execute manufacturing operations in cGMP facility, including: Operate dispensing equipment Operate compounding equipment Operate filling equipment Sample product for release testing Clean ...
The position entails work under general supervision for routine tasks and with detailed instructions on new assignments. Tracking and preparing study-specific information utilizing databases, ...
Top 3 Skills 510K submissions IVD experience Technical background Education: Bachelor's degree required, Masters degree preferred Experience: Minimum of 6 years experience Skills: ...
A highly motivated Research Associate to join the Analytical Development team in Bioanalytics, which develops, validates, and transfers analytical methods used for characterization and release of ...
Must have: Comprehensive understanding of clinical trial operations, including PK, PD, Laboratory Safety testing, and additional protocol assessments terminology. Knowledge of clinical design ...
Looking for an Associate Director Real World Evidence (contractor) that will support various activities in the Solid Tumor and/or Hematology Franchise. As an Associate Director Real World ...
Project Manager Regulatory AffairsSummaryThe function of a Regulatory Affairs Project Manager is to provide Regulatory guidance and support for the US FDA 510(k) Premarket Application for Hematology ...
Looking for a highly motivated Research Associate to join the Biology Core Support group. Responsible for expression, purification and characterization of recombinant proteins and antibodies to ...
The Clinical Quality Improvement Liaison (CQIL) is responsible for managing HEDIS and Stars performance by working with low performing providers to identify areas of opportunity. The CQIL will be the ...
There are 2 positionsABOJP00006524 :: 12 months assignment :: Looking for REACH experience Candidate will be working in the lab 100% of the time. Not a remote opportunity Material Science ...
Assist in monitoring initial phases of medical science studies (including journal reviews, and characterization testing). Independently identify data outliers and prepare data for analysis for ...
