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Field Research Associate
BASINGSTOKE, ENGLAND, UNITED KINGDOM
...opportunity for a Field Research Associate to join our multi-disciplinary R&D Team based at our Head Office in Basingstoke. This role is offered on a hybrid working pattern, with the expectations of two days per week in the office and some ad-hoc travel to our UK clinics as required. What can we...
We've expanded the search to "England" to find more jobs with all your keywords
Senior Regional Clinical Research Associate
LONDON AREA, UNITED KINGDOM, UNITED KINGDOM
The IVD Clinical Research Associate will design, plan, coordinate, and conduct all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. Responsibilities include but are not limited to: Ensuring studies are conducted and documented in...
Senior R&D QA GCP Auditor
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
Background must be in pharma NOT medical devices) Senior R&D QA GCP Auditor (pharmaceuticals) I'm looking to recruit a seasoned Senior R&D QA GCP Auditor responsible for ensuring compliance and proper implementation of Good Clinical Practice (GCP) and Good Clinical Laboratory Practice (GCLP) within...
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MAIDENHEAD
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In Vitro Diagnostics CRA
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
The IVD Clinical Research Associate will design, plan, coordinate, and conduct all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. Responsibilities include but are not limited to: Ensuring studies are conducted and documented in...
Senior R&D QA GCP Auditor
ENGLAND, ENGLAND
...implementation of Good Clinical Practice (GCP) and Good Clinical Laboratory Practice (GCLP) within the clinical development of Global R&D projects in the UK and EU settings. /p p br /p p The ideal candidate should possess substantial experience as a GCP-GCLP auditor in pharmaceutical firms...
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In Vitro Diagnostics CRA
ENGLAND, ENGLAND
p The IVD Clinical Research Associate will design, plan, coordinate, and conduct all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. /p p /p p Responsibilities include but are not limited to: /p p Ensuring studies are...
We've expanded the search to "United Kingdom" to find more jobs with all your keywords
Senior Clinical Research Associate
UNITED KINGDOM, , UNITED KINGDOM
About the job Unique opportunity here to join a small CRO, scaling up their clinical operations team, led by an industry leader that has previously found success in establishing another leading global CRO. Despite being the size of a start-up, they're an established organisation ready for the next...
Clinical Research Associate
SWANSEA, WALES, UNITED KINGDOM
...Investigators and research personnel. Additionally, you will oversee routine close-out activities and conduct thorough audits to ensure compliance at investigative sites. The Role You will be pivotal in overseeing the progress of clinical trials and research endeavours. You will ensure that...
Senior Clinical Research Associate
UNITED KINGDOM, UNITED KINGDOM
p b About the job /b /p p br /p p Unique opportunity here to join a small CRO, scaling up their clinical operations team, led by an industry leader that has previously found success in establishing another leading global CRO. Despite being the size of a start-up, they're an established...
Clinical Research Associate
SWANSEA, SWANSEA
...Investigators and research personnel. Additionally, you will oversee routine close-out activities and conduct thorough audits to ensure compliance at investigative sites. /p p br /p p The Role /p p br /p p You will be pivotal in overseeing the progress of clinical trials and...
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Manager, Clinical Trial Strategy & Submissions, Regulatory Operations
MAIDENHEAD, ENGLAND, UNITED KINGDOM
...submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team and study teams. Ensure study deliverables are achieved in accordance with global regulatory...
Matches: clinical associate, maidenhead
Supply Chain Quality Associate
MAIDENHEAD, ENGLAND, UNITED KINGDOM
Supply Chain Quality Associate - Maidenhead, England - Permanent Proclinical is seeking a dedicated QA Associate for our Supply Chain Quality Assurance team. This is a permanent position located in Maidenhead, England. Primary Responsibilities: The primary focus of this role is to work with...
Matches: associate, maidenhead
Regulatory Affairs Associate
MAIDENHEAD, ENGLAND, UNITED KINGDOM
Role: Regulatory Affairs Associate Location: Maidenhead / M4 corridor. Salary: Very competitive salary on offer Planet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a...
Matches: associate, maidenhead
Quality Assurance Specialist
MAIDENHEAD, ENGLAND, UNITED KINGDOM
...science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It s this combination that makes us different. We re committed to providing...
Matches: clinical, maidenhead
Regulatory Specialist
MAIDENHEAD, ENGLAND, UNITED KINGDOM
SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. The Role: The Regulatory Associate is responsible for providing global...
Matches: associate clinical, maidenhead
Procurement Manager
MAIDENHEAD, ENGLAND, UNITED KINGDOM
...Conduct market research and analysis to identify potential suppliers and products/services, ensuring value for money and quality standards. Lead procurement processes, including tendering, negotiations, and contract management. Collaborate with internal stakeholders to understand their...
Matches: research, maidenhead
QA Manager (GCP)
MAIDENHEAD, ENGLAND, UNITED KINGDOM
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...
Matches: clinical research, maidenhead
Manager, Clinical Trial Strategy & Submissions, Regulatory Operations
MAIDENHEAD, SOUTH EAST ENGLAND
...submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team and study teams. /li li Ensure study deliverables are achieved in accordance with global...
Matches: associate clinical, maidenhead
Supply Chain Quality Associate
MAIDENHEAD, SOUTH EAST ENGLAND
p b Supply Chain Quality Associate - Maidenhead, England - Permanent /b /p p br /p p Proclinical is seeking a dedicated QA Associate for our Supply Chain Quality Assurance team. This is a permanent position located in Maidenhead, England. /p p br /p p b Primary Responsibilities: /b /p...
Matches: associate, maidenhead
Regulatory Affairs Associate
MAIDENHEAD, SOUTH EAST ENGLAND
p b Role: /b Regulatory Affairs Associate /p p b Location: /b Maidenhead / M4 corridor. /p p b Salary: /b Very competitive salary on offer /p p br /p p Planet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join...
Matches: associate, maidenhead
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