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For example, a clinical research physician may next take a job in safety/pharmacovigilance; or in regulatory affairs. Gaining experience in the different positions provides breadth that can be applied to later jobs. After the first several years of experience in the industry, most physicians m...
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1. Identify and evaluate potential strategic partners, including healthcare policy makers, pharmaceutical development whole lifecycle related non-scientific stakeholders & sponsors, that align with the R&D Center's goals and objectives. 2. Develop and implement partnership strategies to support the R&D Ce...
“What I see with pharma companies today is that a person must be an exact functional fit, with all the credentialing, and in the proper therapeutic area. Also, there is a big call to office, which means there are fewer remote accommodations being given to both current and in-coming ...
Posted in cell-based therapy, Drug Discovery Chemistry, FDA, FDA, CE Mark & Global Regulatory Affairs: process management and strategic planning - GCP, GLP, ISO 14155, Pharmaceutical Discovery, Pharmaceutical Drug Discovery, Pharmaceutical R&D Inform...
Cardiovascular disease (CVD) is an emerging contributor to national morbidity and mortality in Saudi Arabia. CVD risk prevention services are limited, particularly with an over-utilised public health sector and an under-utilised and under-resourced prima
6.6 Impact of Evolutionary Selection on Functional Regions: The imprint of Evolutionary Selection on ENCODE Regulatory Elements is Manifested between Species and within Human Populations 6.7 Cardiac Ca2+ Signaling: Transcriptional Control 6.8 Unraveling Retrograde Signaling Pathways ...
impossible to know if a prior invention is lurking that hasn’t yet been filed; as a result, a first-to-invent system inhibits investment in new technology areas.” Chris thinks that first-to-file and the new Act will better enable new technology businesses and new technology jobs. ...