DNAnexus Launches Powerful Data Analysis and Management Solution for the NovaSeq™ Series of Sequencing Systems
R&D Technical Reviewer
Technical Reviewer will review all technical documents, data, protocols, reports, methods, specifications, notebooks for ANDA/NDA filing. This role will be a part of the Research and Development group located at Vernon Hills, IL.
Responsibilities will include
– Reviewing all formulation and analytical studies documents
– Review work of other writers (in-house or consultant) for accuracy, quality, focus, and adherence to format and stylistic requirements, review data to determine the appropriate tabular and textual formats, and the clarity, logic and order of presentation. …
XIFIN Launches Next-Generation Sequencing Module; Expands Genomics-based LIS Workflow
Manager, Good Clinical Practice Support Job
Purpose
* Responsible for providing support to Clinical Trial Management (CTM) with internal review of clinical trial related documentation, active membership to local CTM SOP Committee, and support to all of the CTM Quality and Audit Management Plans. Provide assistance with training and staff development activities as required by the department, including new hire/on boarding training to support a quality mindset within CTM.…
Manager, Clinical Trial Manager Job
Purpose:
Responsible for the operational and financial management of clinical trial planning and execution for assigned projects. Close collaboration with other members within Clinical Trial Management (CTM) and with various functional units of NNI as well as HQ.
RELATIONSHIPS:
Reports to the Senior Manager or Associate Director of Portfolio Management within Clinical Trial Management (CTM).…
Lead Clinical Research Associate Job
PURPOSE:
Responsible for the performance of assigned sites within assigned trials in accordance with Good Clinical Practice (GCP), ICH guidelines, federal regulations and SOPs. Responsible for operational aspects of planning, managing and execution of site performance in accordance with departmental productivity expectations.…
Phlebotomist
Responsible for training and coaching the pheresis staff and facilitating efficient donor flow through the center. Additional duties include performing venipuncture on donors and having a general knowledge of the reception and registration operations.
1 In compliance with Standard Operating Procedures, (SOPs), performs all aspects of the pheresis procedure and plasma collection, including donor set-up, donor monitoring and donor disconnect.…
OCTOBER 17 – 21, 2017: 67th Annual Meeting of the American Society of Human Genetics (ASHG
Genohm at ASHG 2017 in Orlando, FL
Australian Institute of Marine Science Chooses Matrix Gemini LIMS
New Release for the STARLIMS Content Library (Clinical, QM & Forensics)
Isomorphic Software shares a case study on Genohm
Top Workplaces Award given to CSols, Inc. for their Culture of Excellence
Client Management and Reflex Testing Functionality for Clinical and Testing Laboratories Further Enhances CloudLIMS Lite’s Capabilities
Leveraging Cloud Technology to Manage Processes and Data to Maintain High-Quality Storage Services at The University of Sheffield Biorepository
Founded in 2009, the Biorepository at The University of Sheffield is critical for the progress of health-related research. They provide storage services and high-quality human biological samples to research groups for supporting cutting-edge investigation in the areas of oncology and human metabolism; infection, immunity and cardiovascular disease; and neuroscience.Leveraging Cloud Technology to Manage Processes and Data to Maintain High-Quality Storage Services at The University of Sheffield Biorepository
Laboratory Informatics Weekly Update – Volume 15, Issue 38
October 04, 2017 Laboratory Informatics Weekly Update Volume 15, Issue 38 In This Issue Webcast Focus OCTOBER 26, 2017, 1:30PM EDT / 5:30 UTC: Webinar “A Guide for Management: Successfully Applying Laboratory Systems to Your Organization’s Work Part 1” This webinar series is designed as a management level view of laboratory systems and is appropriate for anyone planning, reviewing, or approving the acquisition of laboratory informatics. A background in science is not necessary to follow the webinar material. Its purpose is to provide you with an understanding of how these technologies (Laboratory Information Management Systems, Electronic Laboratory Notebooks, Scientific Data…Data management: New tools, new organization, and new skills in a French research institute
As calls for open scientific data get louder — particularly in Europe — research institutes, organizations, and data management stakeholders are being forced to consider their data management policies and research workflow in an attempt to better answer those calls. Martin et al. of the National Research Institute of Science and Technology for Environment and Agriculture (Irstea) in France present their institute's efforts towards those goals in this 2017 paper published in LIBER Quarterly. They refer frequently to the scientific and technical information (STI) professionals who must take on new skills, develop new policies, and implement new tools to better meet the goals of open data. Martin et al. conclude with five points, foremost that these changes don't happen overnight; the necessary change "requires adaptation to technological developments and changes in scientific practices" in order to be successful.
Lab Systems Technologist
The lab information system technologist participates in system analysis, computer security, results retrieval/transmittal to and from remote facilities, billing, compliance, interfacing anatomic and clinical pathology systems to the hospital information system, and interfacing to systems off-campus clients and reference laboratories. The purpose of the position is to enable accurate, speedy, customer-focused and cost effective data distribution and information generation to optimize patient care.…
Technical Writer- Life Sciences
Covance's BioAnalytical lab is seeking a Life Sciences Technical Writer for their Early Development- BioAnalytical, Chantilly, VA site. 3-4 years of study coordinator experience required, nonclinical preferred.
Responsibilities:
– Drafts protocols, sample analysis outlines (SAOs), amendments and study schedules as appropriate, using proposal outline or client-supplied information. …
