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Medical Writer
MANCHESTER AREA, UNITED KINGDOM, UNITED KINGDOM
...account lead(s)/line manager at the earliest stage any potential barriers to successful project completion and suggests solutions Play a pivotal role within the editorial team, always leading by example and demonstrating knowledge of good practice/industry guidelines Recognise where s/he can...
Medical Writer
MANCHESTER
...account lead(s)/line manager at the earliest stage any potential barriers to successful project completion and suggests solutions /li li Play a pivotal role within the editorial team, always leading by example and demonstrating knowledge of good practice/industry guidelines /li li Recognise...
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Senior MRI Radiographer
£35,617 - £44,000 a year
OXFORD, ENG, GB
...partnership with the Clinical Lead and Perspectum to ensure we are aligned in every aspect of the service. Perspectum is active in developing quantitative imaging techniques using machine learning and there will be a great opportunity to get involved with research projects and commercial trial...
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Senior Associate/Manager, Disclosure, Global Clinical Trial Transparency - 12 Month FTC
41885
HATFIELD, HERTFORDSHIRE, HATFIELD, HERTFORDSHIRE, AL10 9SN
Job description: Senior Associate/Manager, Disclosure, Global Clinical Trial Transparency - 12 Month FTC The Company Eisai is a leading research based pharmaceutical organisation with an extensive portfolio across the Oncology, Neurology and Pain therapy areas. By joining Eisai, you will be working...
Clinical Trial Coordinator (Central London - Hybrid) - UK - FSP - REGISTER YOUR INTEREST
33569
UXBRIDGE, LONDON , UXBRIDGE, LONDON
We are inviting applications to join our UK Clinical Trial Coordinator talent pipeline and a chance to play a pivotal role in some of the most significant clinical studies taking place today Please provide some basic information and upload your CV . Hybrid working, with a central-London based...
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Global Clinical Trial Transparency & Disclosure Manager
44658
ENGLAND, HERTFORDSHIRE, HERTFORDSHIRE, UK, HERTFORDSHIRE, HERTFORDSHIRE
An opportunity has opened to support one of our established Pharma client's Global Clinical Trial Transparency disclosure operations in a 12 month, FTC (fixed term contract). You'll ensure compliance with the disclosure processes which support the company's Policy for Clinical Trial Transparency...
Global Clinical Trial Transparency Manager - Disclosure
49981
HATFIELD, HERTFORDSHIRE, HATFIELD, HERTFORDSHIRE
Planet Pharma are currently partnered with a leading global pharmaceutical company who are seeking a Global Clinical Trial Transparency Manager to join their Disclosure Team on an initial 12 month contract. You ll be a part of a great team of cross functional professionals working with various...
Director, Program Operations Leader, Early Clinical Trial Development
45725
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...complex programs in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and decisions including quality, timelines and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and...
Senior Clinical Data Manager - single sponsor
41408
MAIDENHEAD, BERKSHIRE, MAIDENHEAD, BERKSHIRE
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 device customers a wide range of clinical development, patient access and technology solutions...
Assoc Mgr Clinical Study
60833
UXBRIDGE, LONDON , UXBRIDGE, LONDON
This role is a hybrid position which means the individual must work on-site 3 days per week. Fully remote work is not possible for this role. The position can be based in Armonk, NY or Basking Ridge, NJ. A Clinical Study Associate Manager (CSAM) role supports the Clinical Study Lead (CSL) by taking...
Experienced Clinical Research Associate
45784
READING, BERKSHIRE, READING, BERKSHIRE
...i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability Administer protocol and related study training to assigned sites...
Financial SSU PM (home-based)
50958
MAIDENHEAD, BERKSHIRE, MAIDENHEAD, BERKSHIRE
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 device customers a wide range of clinical development, patient access and technology solutions...
Volunteer Screening Coordinator, Leeds
LEEDS, WEST YORKSHIRE, LEEDS, WEST YORKSHIRE
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 device customers a wide range of clinical development, patient access and technology solutions...
Senior Director, Global Patient Safety - Ophthalmology
61932
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.) Leads cross-functional Safety Monitoring Team (SMT) activities Represent GPS for assigned compounds on cross-functional teams, including Regeneron s Safety Oversight Committee (RSOC...
Senior Director, Global Patient Safety - Gene Therapy
62571
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...provide PV input for clinical documents (Investigator Brochures, protocols, clinical study reports, and other relevant study documents) Lead cross-functional meetings including Safety Monitoring Team (SMT) activities Represent GPS for assigned compounds on cross-functional teams, including...
Director, Global Patient Safety Sciences - Hematology
80469
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.) Leads cross-functional Safety Monitoring Team (SMT) activities Represent Global Patient Safety for assigned compounds on cross-functional teams, including Regeneron s Safety Oversight...
Senior CRA (Hematology)
66851
READING, BERKSHIRE, READING, BERKSHIRE
Our cFSP (sponsor dedicated) team are growing join us on our mission to drive healthcare forward We are recruiting for a Senior Clinical Research Associate / Senior Clinical Research Associate II to assist our sponsor s hematology studies. Why IQVIA? Growth potential - clear pathways to success...
Contract Senior Manager, Global Trial Optimisation
LONDON, ENGLAND, UNITED KINGDOM
Proclinical is seeking a dedicated Manager of Global Trial Optimisation. This role involves overseeing the clinical development strategy, clinical study concepts and protocols as well as operational plans. The successful candidate will play a crucial part in maintaining relationships with external...
Regulatory Affairs Manager (UK/I) Contract
not provided
CAMBRIDGE, CAMBRIDGESHIRE, EAST ANGLIA, UK
Your new company A global biopharmaceutical company is looking to bring on a Regulatory Affairs Manager to support the UK&I team. Your new role This is a varied role and as the Regulatory Affairs Manager you will be responsible for supporting the clinical trial applications, PIP's, or...
Clinical Trial Manager
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
Your New Company Experienced Clinical Trial Manager for Global Pharma, remote based position, must have previous CRA experience - imm start Acts as Country Study Manager for designated studies as required by the Director of Clinical Operations Responsible for the local portion of the assigned study...
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