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We need resource on day shift and on night shift. The days are Friday, Saturday, Sunday, and Monday. The shifts are 10 hours, and the exact hours are listed below.Day Shift: 6:00 AM – 4:30 ...
The Consultant will be based in Summit, NJ and will assist the Regulatory-CMC Biologics/Cell Therapy team with projects to support department goals and objectives. Responsibilities: Attention ...
Job Description: Masters degree with research experience will work for this role Lab experience needed 1 - 2 yrs PCR experience is a must have Core job responsibilities include qPCR, flow ...
2nd shift (3 pm to 11 pm), after training period on 1st shift Some experience analyzing blood samples in a laboratory environment, working in GLP area preferred Minimum B.S. in Medical ...
Description: Plan, direct, or coordinate clinical research projects. Direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall ...
Global Service Technical Operations - Customer Service TechnologistSummary Applies subject matter knowledge in the area of Medical Device Field Service. Experienced professional individual ...
This is a short term 3-4 month assignment for two openings, team has extra budget for a short term project for which they need help. JD is short, more details will be shared on the ...
The Aseptic Quality Operations group supports the onsite small scale commercial manufacturing facility. The QC Microbiology Laboratory Technician conducts routine sampling and testing of ...
Tracking and preparing study-specific information utilizing databases, spreadsheets, and other tools Provide input and assist with harmonization of Clinical Operations databases and tracking ...
Contributes to the preparation and submission of regulatory filing documents. Monitors and tracks information and requirement changes. Major Accountabilities: Provides assistance to members ...
Candidates will be working remote foreseeable future. Person could remain remote for the duration of the assignment. Running remediation activities in a regulatory affairs Working with 15-20 ...
The Chemical Plant R&D Technician will provide testing of raw materials, intermediates, and finished products, in a safe manner, for the client Corp within the scope of the ISO 9001 procedures ...
Biophysics ScientistThe candidate will work within the biophysics group on the application of binding assays in support of the discovery of therapeutic candidates. The focus of this position will be ...
Must meet all requirements for Clinical Trials Management Associate (CTMA) position and must have demonstrated proficiency in all relevant areas Serves as the key operational contact with external ...
Perform operations necessary for quality testing and plays a role in implementing new technology within quality control. At more senior levels, provide an investigative or technological orientation ...
Manage front desk activities to include greeting patients, scheduling appointments, medical record management, photocopying, correspondence, answering phones and entering medical data into the ...
The Process Technician supports the execution of Commercial, Clinical, and/or Development production according to Standard Operating Procedures and Production Schedule. The Process Technician ...
The Pharmacovigilance (PV) Scientist role works collaboratively with the Global Safety Physician (GSP) and (Senior/Principal) PV Scientist with the review of safety data and related documents for ...
Client is seeking a highly motivated and innovative Research Associate to join the Antibody and Protein Engineering Group in the Discovery Biotherapeutics Department in San Diego. The ...
