Contract Clinical Research Jobs

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 - 5 days ago

SRG - Dublin, Republic of Ireland

Supporting pharmacovigilance activities (e.g., reviewing/contributing to aggregate reports/patient narratives, attendance of Safety Monitoring Meetings - if required Basic knowledge in planning, executing... £12.95 - £17.26/hour

from: CV-library.co.uk - 16 days ago

Parexel - United Kingdom

Together with Project Leader ensure all administrative closeout procedures are completed according to Project Close-out Checklist, project is archived, and all documentation returned to the client as specified...

from: jobleads.co.uk (+1 source) - 3 days ago

Medpace - London, England, 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...

from: jobleads.co.uk (+1 source) - More than 30 days ago

Medpace - Stirling, United Kingdom (+1 location)

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 - 22 days ago

Medpace - London, England, 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...

from: jobleads.co.uk (+1 source) - More than 30 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) - 22 days ago

ARTO - London, United Kingdom

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: uk.lifeworq.com - 25 days ago

BioTalent - London, United Kingdom

CRA being appointed to secure sample forecast, assist with monitoring on the study and data cleaning as well as support with due diligence monitoring on the first in human programme (FiH). BioTalent Ltd...

from: uk.lifeworq.com - 4 days ago

Fortrea - Yorkshire, UK

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical... not provided

from: totaljobs.com - 10 days ago