Head of Regulatory Strategic Medical Writing
This position is responsible for developing and implementing a vision for and leading the Regulatory Strategic Writing (RSW) team within Regulatory Affairs. In partnership with the Global Regulatory Product Team (GRPT), the RSW team drives the compilation and preparation of global critical strategic regulatory submission documents comprised of high quality, scientific justification, and relevant regulatory style/reference for submission to global health authorities to support product priorities. …
Associate Clinical Development Medical Director
The Associate Clinical Development Medical Director (Assoc. CDMD) is responsible for the scientific and medical strategy of assigned clinical trial(s), medical and scientific monitoring, and reporting of quality data. May be responsible for the scientific and medical strategy of assigned sections of a clinical development program, depending on the size and complexity. …
Senior Director, R&D
If you're inspired by the possibilities of science to change lives and you thrive when making brave decisions – join us.
MedImmune is the worldwide biologics research and development arm of AstraZeneca. Here, you'll have the opportunity to make a difference in people's lives every day.…
Medical Lab Scientist
At UCHealth, we do things differently
We believe in something different: a focus on the individuality of every person. In big ways and small, we exist to improve the extraordinary lives of all those we serve. As Colorado’s largest and most innovative health care system, we as a team deliver on the commitment to provide the best possible experience for our patients and their families.…
Italian Murder Case Wins The 2017 DNA Database Hit Of The Year Award
Pathology Informatics Summit – Visit Abbott Informatics at Booth #12
Blow Fill Seal (BFS) Pharmaceutical Manufacturing Technician
The Pharmaceutical Manufacturing Technician, Blow Fill Seal will be responsible for the set up, operation and cleaning of all pharmaceutical manufacturing/packaging equipment including; Rommelag Blow Fill Seal machine, sterilizer and labeling equipment. Personnel in this position will operate manufacturing processing equipment by following standard operating procedures and batch records in accordance with FDA current Good Manufacturing Practices.…
MAY 27 – 30, 2017: European Human Genetics Conference 2017
JUNE 18 – 22, 2017: DIA 2017 Annual Meeting
JULY 30 – AUGUST 3, 2017: 69th AACC Annual Scientific Meeting & Clinical Lab Expo
AUGUST 28 – 30, 2017 Cannabis Science Conference
Global Lead, Clinical Trial Disclosure and Transparency Lead
The Global Lead, Clinical Trial Disclosure and Transparency is a key leadership position responsible for providing strategic leadership, development, and management of CSLs global Clinical Trial Disclosure and Transparency function. The incumbent will lead and develop the group responsible for clinical trials registration, summary results disclosure, data disclosure and transparency responsibilities in all regions across the global CSL organization according to CSL policy. …
Senior Scientist – Sterile Liquid Commercialization
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its 125-year legacy.…
ATUM Licenses Gene Design Software to Thermo Fisher Scientific
Genohm at #eshg2017 in Copenhagen
SLims by Genohm integrated with Pathomation’s PMA.core
Assay Development Associate – Vector Shedding/Bio Distribution
The Assay Development Associate – Vector Shedding/Bio Distribution will:
•With guidance and supervision from the group leader or supervisor, conduct clinical and preclinical sample analysis per SOPs and generate data with high scientific quality to meet GLP regulatory expectations.
•Participate in validation of bioanalytical assays such as immunoassays and cell-based assays. …
Manager of Quality Assurance Validation
Summary
The role of the QA Validation Manager is to ensure compliance with company and regulatory requirements e.g. Good Manufacturing Practices (GMP), Code of Federal Regulations (CFR) and local regulations. The QA Validation Manager, directly reporting to the Quality Director, manages the QA Validation Specialists, coordinates and schedules all activities to assure that all new or existing pieces of equipment, utilities, instruments, analytical methods and processes are adequately qualified and validated in accordance with the requirements outlined in the approved Validation Master Plan requirements, the approved validation test protocol, applicable policies and procedures, through review of the aforementioned documentation and collaboration with the responsible party. …
Laboratory Informatics Weekly Update – Volume 15, Issue 20
May 24, 2017 Laboratory Informatics Weekly Update Volume 15, Issue 20 In This Issue Webcast Focus JUNE 21, 2017 2:00PM EDT/6:00PM USTC: ELN Implementations - Why they Fail to Realize their Full Potential! Join us for this one hour, complimentary webinar in which we examine the reasons why ELNs fail to realize their full potential and what can be done to improve your chances of success. Event Focus MAY 22 - 24, 2017: Clinical Trial Supply Logistics & Temperature Management Forum Leading experts will discuss the future of clinical trials for 2017 and beyond! Don’t miss this key event to…Selecting a laboratory information management system for biorepositories in low- and middle-income countries: The H3Africa experience and lessons learned
What's important for a biorepository laboratory information management system (LIMS), and what options are out there? What unique constraints in Africa make that selection more difficult? This brief 2017 paper from the Human Heredity and Health in Africa (H3Africa) Consortium outlines their take on finding the right LIMS solution for three of their regional biorepositories in Africa. The group emphasizes in the end that "[c]hoosing a LIMS in low- and middle-income countries requires careful consideration of the various factors that could affect its successful and sustainable deployment and use."
