Clinical Research Contract Jobs in Uxbridge

CK Group- Science, Clinical and Technical - Slough, United Kingdom

The successful applicant will be responsible for planning and technical oversight of Biomarker Transcriptomics activities outsourced to CROs. Experience working with Contract Research Organisations (CROs)... £0 - £20.03/hour

from: CV-library.co.uk (+1 source) - 16 days ago

KINGS COLLEGE LONDON - London (Central), London (Greater), England

- To assist the Quality Manager (QM) and R&D staff in the partner institutions to ensure that all trials sponsored or co-sponsored by the partner organisations are conducted in accordance with the current... £43,205 - £50,585 per annum, including London Weighting Allowance

from: timeshighereducation.com (+1 source) - More than 30 days ago

Fortrea - Maidenhead, United Kingdom

Key words: Clinical Research, SCRA, Clinical Research Associate, London GCP, Monitor, Monitoring, Senior Clinical Research Associate, CRA I, Oncology, Field Based, Home Based, CRO, Pharmaceutical, London... Competitive

from: pharmiweb.jobs - 9 days ago

London, England, United Kingdom

The Site Support Manager (SSM) position is responsible for performing and overseeing image quality checking (QC) and resolving site and data issues for clinical data received by IXICO in active clinical...

from: jobleads.co.uk - 5 days ago

Medpace - London, United Kingdom

This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position... Competitive

from: pharmiweb.jobs (+1 source) - 8 days ago

Medpace - London, United Kingdom

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will... Competitive

from: pharmiweb.jobs (+1 source) - 8 days ago

ARTO - London EC1A, City of London, London

Prepare and review study-related documentation, including informed consent forms, case report forms (CRFs), study reports, and regulatory submissions, to ensure compliance with applicable regulations and...

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

Medpace - London, United Kingdom

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will... Competitive

from: pharmiweb.jobs - 8 days ago

Medpace - London, United Kingdom

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will... Competitive

from: pharmiweb.jobs - 8 days ago

CYTE Global - London EC1A, City of London, London

Clinical Data Manager will ensure CYTE studies are planned and implemented to the highest standards, in compliance with ICH-GCP guidelines, CYTE SOPs and all applicable regulatory guidelines. Creation...

from: joblookup.com (+1 source) - 8 days ago