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Clinical Trial Operations Specialist
BRACKNELL, ENGLAND, UNITED KINGDOM
CLINICAL TRIAL OPERATIONS SPECIALIST 12 Months Contract OUR COMPANY At Boehringer Ingelheim we develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned company, we focus on long-term performance. We believe...
Clinical Trial Operations Specialist
BRACKNELL, SOUTH EAST ENGLAND
p b CLINICAL TRIAL OPERATIONS SPECIALIST /b /p p br /p p 12 Months Contract /p p br /p p b OUR COMPANY /b /p p At Boehringer Ingelheim we develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned...
Clinical Trial Operations Specialist
BRACKNELL
p strong CLINICAL TRIAL OPERATIONS SPECIALIST /strong /p p br br Not sure what skills you will need for this opportunity Simply read the full description below to get a complete picture of candidate requirements. br /p p 12 Months Contract /p p br /p p strong OUR COMPANY /strong /p p...
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Clinical Research Associate
£40000 - £60000/annum
OX11, DIDCOT, OXFORDSHIRE, OX11
Cure Talent are delighted to be partnered with an established Medical Devices Manufacturer, who, due to their continued growth, have an exciting opportunity for an experienced Clinical Research to join them. As the new Clinical Research Associate, you will be responsible for overseeing trial sites...
Regulatory Manager, Clinical Trial Strategy & Submissions
MAIDENHEAD, GB
We re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead/hybrid. The Role: Deliver CTA...
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Manager, Clinical Trial Strategy & Submissions, Regulatory Operations
MAIDENHEAD, GB
...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...
Regulatory Specialist
MAIDENHEAD, GB
...expertise for Clinical Trials. They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes. Key Responsibilities: Manage a portfolio of CTAs including preparation and distribution of documentation...
Senior/Principal HTA Statistician
WOKINGHAM, GB
...medicine by analysing clinical trial data, providing statistical consultancy, and mentoring junior colleagues. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities Apply innovative statistical approaches to solve novel data...
Project Manager
SLOUGH, GB
Life Sciences Recruitment is pleased to confirm that we are working with our global, fast-growing clinical trial supply (CTS) client, to hire a Project Manager to join their Unlicensed Medicines division. For this position, you will be a key point of contact for new & existing clients for the...
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...
Regulatory Specialist
MAIDENHEAD, SOUTH EAST ENGLAND
...expertise for Clinical Trials. They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes. /p p /p p b Key Responsibilities: /b /p ul li Manage a portfolio of CTAs including preparation...
Senior/Principal HTA Statistician
WOKINGHAM, SOUTH EAST ENGLAND
...medicine by analysing clinical trial data, providing statistical consultancy, and mentoring junior colleagues. /p p /p p Please note that to be considered for this role you must have the right to work in this location. /p p b /b /p p b Key Responsibilities /b /p ul li Apply...
Regulatory Manager, Clinical Trial Strategy & Submissions
MAIDENHEAD
p We’re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead/hybrid. /p p br br...
Manager, Clinical Trial Strategy & Submissions, Regulatory Operations
MAIDENHEAD
...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...
Regulatory Specialist
MAIDENHEAD
...expertise for Clinical Trials. They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes. /p p strong u Key Responsibilities: /u /strong /p ul li Manage a portfolio of CTAs including...
Project Manager
SLOUGH
p Life Sciences Recruitment is pleased to confirm that we are working with our global, fast-growing clinical trial supply (CTS) client, to hire a Project Manager to join their Unlicensed Medicines division. /p p br br Find out more about this role by reading the information below, then apply to...
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Regulatory Affairs Associate (EU)
SURREY, GB
Regulatory Affairs Associate The Regulatory Affairs Associate will be responsible for: Managing the clinical trial applications in Europe and other selected countries Keeping up to date with regulatory and legal changes in EU Preparing pre- and post-authorisation regulatory documentation and...
Regulatory Affairs Coordinator
MARLOW, GB
...experience ideally in clinical trials and CTR submission experience would be preferred. Job Responsibilities include a portfolio of CTAs including preparation and distribution of documentation associated with new initial CTAs and all CTA maintenance activities such as substantial amendments...
Senior Data Analyst - Biotechnology
OXFORDSHIRE, GB
...scale biological and clinical datasets. Collaborate closely with interdisciplinary teams including researchers, bioinformaticians, and software engineers to design and execute data-driven experiments and analyses. Develop predictive models and algorithms to support drug discovery, biomarker...
Senior Bioinformatician
OXFORDSHIRE, GB
...transcriptome, and clinical or experimental factors. Utilise machine learning methods, such as supervised and unsupervised learning, to merge multi-omics data and pinpoint predictive biomarkers related to immune response and disease prognosis. Cultivate robust collaborations with...
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