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IQVIA - reading, england, United Kingdom
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data...
from: jobleads.co.uk (+1 source) - 9 days ago
reading, england, United Kingdom
Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines...
from: jobleads.co.uk - 5 days ago
SRG - Marlow, United Kingdom
To compile & review batch document sets for completeness & compliance to EU GMP, Pfizer internal requirements and regulatory dossier submissions. SRG are working with a Global Consumer Pharmaceutical company...
from: uk.lifeworq.com - 4 days ago
IQVIA - reading, england, United Kingdom
Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines...
from: jobleads.co.uk (+1 source) - 7 days ago
Johnson and Johnson - High Wycombe
* Within Clinical Data Standards: Data Collection Standards, Data Delivery Standards, Data Analysis Standards, Submissions and Regulatory Intelligence, Data Standards Planning. Outside Clinical Data Standards...
from: Johnson and Johnson - 9 days ago
Basingstoke, England, United Kingdom
This role will report to the Director, Global Learning & Development. The Talent Development team is focused on being exceptional business partners who deeply know the business and develop impactful, yet...
from: jobleads.co.uk - 23 days ago
OMass Therapeutics - Oxford, England, United Kingdom
Experience leading and facilitating the identification, visualization, and acceleration of the project’s critical path, including the ability to explain the critical path activities and dependencies to...
from: jobleads.co.uk (+1 source) - 21 days ago
reading, england, United Kingdom
Apply locations Reading, Berkshire, United Kingdom Solna, Sweden Amsterdam, Netherlands Barcelona, Spain Sofia, Bulgaria time type Full time posted on Posted 7 Days Ago job requisition id R1398680 Ensures...
from: jobleads.co.uk - More than 30 days ago
reading, england, United Kingdom
Ability to write scientific documents e.g. Investigational Medicinal Product Dossier, clinical trial justifications with minimum support of senior staff Prepares and/or reviews regulatory documents to...
from: jobleads.co.uk - More than 30 days ago
reading, england, United Kingdom
Manage multiple Regulatory Submissions translation and localization projects at any one time from receipt to completion Experience working with TMS and CAT tools, experience working with XTRF and/or memoQ...
from: jobleads.co.uk - More than 30 days ago