iSpecimen® Announces Data Connector Program to Seamlessly Connect Biospecimen Providers to the iSpecimen Marketplace
Holiday Planning Tips for a Joyous LIMS Project
Let’s explore some of the holiday planning and preparation tactics that can be leveraged to help make your LIMS project a true celebration.Holiday Planning Tips for a Joyous LIMS Project
Compliance culture or culture change? The role of funders in improving data management and sharing practice amongst researchers
In this 2017 paper by Curtin University's Cameron Neylon, the concepts of research data management (RDM) and research data sharing (RDS) are solidified and identified as increasingly common practices for funded research enterprises, particularly public-facing ones. But what of the implementation of these practices and the challenges associated with them? Neylon finds more than expected in his study, identifying sharp contrast among "those who saw [data management] requirements as a necessary part of raising issues among researchers and those concerned that this was leading to a compliance culture, where data management was seen as a required administrative exercise rather than an integral part of research practice." Neylon concludes with three key recommendations for researchers in general should follow to further shape how RDM and RDS are approached in research communities.
Labware LIMS System Admin
LabWare LIMS Sr Sys Admin
This role primarily requires:
1A. Basic BA skills are a nice to have, but will not be required to gather requirements, must have script clean up experience, knowledge of off-the-shelf vs custom Labware changes to guide business in the appropriate path forward, and be able to implement changes independently to existing functionalities as well as implement new applications within Labware. …
Labware LIMS System Admin
LabWare LIMS Sr Sys Admin
This role primarily requires:
1A. Basic BA skills are a nice to have, but will not be required to gather requirements, must have script clean up experience, knowledge of off-the-shelf vs custom Labware changes to guide business in the appropriate path forward, and be able to implement changes independently to existing functionalities as well as implement new applications within Labware. …
Respiratory Medical Science Liaison/Sr. MSL
At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. We're focused on the potential of science to address the unmet needs of patients around the world.…
Sr. Director, R&D
This is an important, high profile and visible role and requires an individual with outstanding communication and cross-functional leadership skills, as well as the ability to build strong relationships with key stakeholders in Clinical and other relevant functions within MedImmune and external academic collaborators.…
Global Principal Clinical Scientist
The position holder is responsible for both scientific input to clinical development strategies for early pipeline projects, acting as a liaison between Research, clinical Development Therapeutic Area and key stakeholders to ensure translation of the development plan into operational deliverables. Contribution to the scientific content of clinical program documents is a key deliverable and includes the Early Development Plan, study synopses and protocols, Investigator’s Brochures, clinical study reports, conference abstracts, internal and external scientific meeting presentations and peer-reviewed publications
Main Responsibilities and Accountabilities
1 Contribute, in collaboration with Research, the scientific rationale for clinical development strategies for early pipeline programs.…
Temporary Technical Writer – Analytical
Overview
3 Month Assignment.
Prepare documentation to include specifications, method verification/validation reports, method transfer reports, and characterization reports as and when needed in appropriate format required by regulatory affairs.
Review, revise and draft Standard Operating Procedure documents.
Working efficiently to setup Active Pharmaceutical Ingredients (API) as well as Finished Product (FP) specification based on API manufacturers drug master file (DMF), United state Pharmacopeia (USP) monograph and ICH guidelines with the help of group leader and scientist. …
