Principal Writer Jobs

Precision AQ - United Kingdom

Maintains current knowledge (e.g. conducts literature searches) regarding competitor products, drugs in development, treatment, and strategic issues for assigned therapeutic area(s) to ensure delivery... Competitive

from: newscientist.com - 12 days ago

Cognite - City of London, United Kingdom (+1 location)

In the fast-changing world in which our clients seek to deliver life-changing medicines and technology, Cognite’s dynamic and forward-thinking team drives us in our mission of bringing science to life...

from: uk.lifeworq.com (+1 source) - 16 days ago

London, England, United Kingdom

Bachelor’s, Masters or PhD Degree in scientific, medical, clinical discipline or related field is required with at least 6 years of previous regulatory writing experience; Masters or Phd degree is preferred...

from: jobleads.co.uk - 16 days ago

Cognite - London, United Kingdom

In the fast-changing world in which our clients seek to deliver life-changing medicines and technology, Cognite’s dynamic and forward-thinking team drives us in our mission of bringing science to life...

from: uk.lifeworq.com - 19 days ago

ICON Strategic Solutions - Any Emea Location, United Kingdom, Homeworking (+1 location)

Clear understanding of clinical development, including the phases, processes, and techniques used within a clinical development environment from protocol design through regulatory submission and support... Competitive

from: pharmiweb.jobs (+2 sources) - 16 days ago

X4 Life Sciences - London EC1A, City of London, London (+1 location)

Play a pivotal role in developing and maintaining our best practices, protocols, and guidance documents. Is your CV ready If so, and you are confident this is the role for you, make sure to apply asap... 125.00-150.00 day

from: joblookup.com (+2 sources) - 18 days ago

JR United Kingdom - London EC1A, City of London, London

Do not wait to apply after reading this description a high application volume is expected for this opportunity. Please apply via this advertisement. We will contact you shortly if your application is successful... 125.00-150.00 day

from: joblookup.com - 5 days ago

cardiff, wales, United Kingdom

Demonstrated expertise of developing value and reimbursement dossiers, value stories, objection handlers, posters, slide decks, report and peer-reviewed publications. Manage project timelines and budgets...

from: jobleads.co.uk - 29 days ago

Bioscript Group - Nottingham NG1, Nottinghamshire, East Midlands (+2 locations)

Lead and motivate regulatory writing team members, adhering to company policies and procedures. Coach and mentor more junior team members, providing support and guidance on client and project-related issues...

from: joblookup.com - 12 days ago

Coronado Research - London EC1A, City of London, London

Participate in interpreting and planning data presentation for individual study reports and summary documents for nonclinical and clinical programs. Ensure all documents comply with regulatory requirements... 125.00-150.00 day

from: joblookup.com - 3 days ago