Job Title QC Associate Job ID 24 02046 Location Devens, MA Duration 06 Months contract on W2 Onsite, Devens Work Schedule Mon Fri, Business Hours This position will perform routine testing including media and reagent preparation, cell maintenance and working closely with several instrumentations used for Bioassay testing. Education and Experience Required BS with minimum

Research Assistant available in Human Neuroimaging Department at Mass. Eye and Ear at our Main Campus, 243 Charles Street, Boston, 02114. Main Campus 40 hours per week with benefits. The Simonyan Laboratory at Massachusetts Eye and Ear and Harvard Medical School () has open positions for one research assistant. The lab's primary research focus is on understanding brain me

In this role, you will serve as an individual contributor within a team; upon the direction and guidance of leadership, you will be responsible for supporting the goal of meeting scope, schedule and delivery requirements. Primary expectations of a Researcher I include Responsible for outreach, recruiting, screening, scheduling, and tracking of research participants Plans

Overview The Department of Infectious Disease and Global Health combines four important areas of expertise within Tufts Cummings School of Veterinary Medicine. These are public/population health, international medicine, wildlife and conservation medicine and infectious disease research. The alignment of these areas promotes cross disciplinary strengths that are important

Hybrid opportunity for a Senior Scientist, Nonclinical Safety Evaluation (NSE). You will be responsible for ensuring timely and high quality deliverables from NSE to meet the organization's discovery and development goals. This job is part time 20 hours per week, located in Waltham, MA Compensation $82.00 $85.00 per hour W2 Review and QC NSE study protocols, study reports

Senior Scientist LC MS Applications Req. # 20243 Company Name Waters Division Category Research and Development Location US Type Regular Full Time Overview This is an outstanding chance for an enthusiastic scientist to join a laboratory based, development team that is working on chromatographic and mass spectrometric tools for the analysis of gene therapy drug products in

Utilize MS Access, Excel and REDCap to assist in data collection efforts, database development, and descriptive data analysis. (In house REDCap and MS Access training is available.) Assist with preparation of Institutional Review Board(IRB) documentation and forms for study protocol approvals and amendments. Schedule conference calls; prepare agendas and pre meeting mater

1. Under general supervision, performs a variety of routine tests following established methodologies. Routine tests may include isolation of running flow cytometry on isolated samples and RNA/DNA isolation. 2. Prepares and maintains tissue cultures. 3. Record data, summarizes, and analyzes results using basic statistics. 4. Prepares laboratory reagents, chemicals, instru

Liaising and collaborating with external entities as experts in immunology. Attending and participating in project team meetings, and coaching research associates. Collaborating with team members to design experiments, and playing a creative role in problem solving. Evaluating promising immunotherapy strategies by planning, creating, and validating cell based and in vivo

The Clinical Research Specialist coordinates and oversees the implementation of recruitment and other operations activities for multiple, concurrent clinical research studies/trials, with responsibilities including Program Communication Strategize with staff when problems arise and offer potential solutions. Ensure uniform application of regulatory requirements across all

Identifying and recruiting patients to participate in research Attending patient appointments and procedures to collect research samples and data Processing, storage, and management of biospecimens from study participants Maintenance of regulatory documentation for all study participants Medical chart review and data abstraction Study and protocol coordination, revision,

Perform administrative support duties to assist the investigative team Attend individual and team meetings Conduct literature review and library searches Assist with developing and managing IRB protocols for the study Assist with recruiting patients for clinical trials Verify subject inclusion/exclusion criteria Provide basic explanation of study and obtains informed cons

The Study Coordinator is responsible for on and off site study implementation and data management of clinical research studies at both domestic (Boston) and international (South Africa) sites. Responsible for development and oversight of study documentation (i.e., protocols, data management and clinical quality management plans, standard operating procedures, informed con

Summary Under supervision and following established policies and procedures conducts experiments using in vivo/or in vitro techniques. Performs minor surgery on animals. Operates monitoring equipment; collects and analyzes data using statistical methodology. Reviews literature in the field for informational purposes or to gather data. Responsibilities Calibrates and sets

The Pathology Technologist reports to the Pathology Manager. Under general supervision and within department policies and procedures performs various complex clinical laboratory tests in one or more of the laboratory sections of the Pathology Department. Work requires a professional level of knowledge in order to read and interpret test results especially those which are