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Senior/Principal HTA Statistician
WOKINGHAM, ENGLAND, UNITED KINGDOM
...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...
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...
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Clinical Trial Operations Specialist
BRACKNELL, GB
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...
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Clinical Trial Manager
MAIDENHEAD, GB
...deliverables for global clinical trial applications in accordance with the overarching global regulatory strategy considering regional specific requirements Coordinate submission strategies for global clinical trials, ensuring alignment with regulatory strategies, and promptly highlighting any...
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...
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Clinical Trial Specialist
MAIDENHEAD, GB
...affairs within clinical trials. Responsibilities: Oversee a portfolio of CTAs, managing the preparation and dissemination of documentation for new initial CTAs and all CTA maintenance activities, including substantial amendments and end-of-trial notifications. Offer guidance on...
Regulatory Affairs Consultant
SLOUGH, GB
...related aspects of clinical trials. You will serve as the main point of contact and be responsible for delivering submission-specific milestones while offering guidance on submission strategies. Additionally, you will actively participate in EU-CTR consulting and contribute to the operational...
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...
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...
Clinical Trial Manager
MAIDENHEAD
...deliverables for global clinical trial applications in accordance with the overarching global regulatory strategy considering regional specific requirements /li li Coordinate submission strategies for global clinical trials, ensuring alignment with regulatory strategies, and promptly highlighting...
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...
Clinical Trial Specialist
MAIDENHEAD
...affairs within clinical trials. /p p strong Responsibilities: /strong /p p • Oversee a portfolio of CTAs, managing the preparation and dissemination of documentation for new initial CTAs and all CTA maintenance activities, including substantial amendments and end-of-trial...
Regulatory Affairs Consultant
SLOUGH
...related aspects of clinical trials. You will serve as the main point of contact and be responsible for delivering submission-specific milestones while offering guidance on submission strategies. Additionally, you will actively participate in EU-CTR consulting and contribute to the operational...
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 Key Responsibilities: /strong /p p Manage a portfolio of CTAs including preparation and...
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 Affairs Consultant
SLOUGH, SOUTH EAST ENGLAND
...related aspects of clinical trials. You will serve as the main point of contact and be responsible for delivering submission-specific milestones while offering guidance on submission strategies. Additionally, you will actively participate in EU-CTR consulting and contribute to the operational...
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...
Regulatory Manager, Clinical Trial Strategy & Submissions
£65 - £75/hour
MAIDENHEAD, BERKSHIRE, SL6
...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...
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Chief Medical Officer/Chief R&D Officer - Africa Clinical Research Network
OXFORDSHIRE, GB
Location: UK-Oxford/London or location in Africa to begin with. Will also consider a remote based contractor. This role may require relocation to African HQ at some point in the future. Hours: Full-time Reports to: Chief Executive Officer - Africa Clinical Research Network Our Mission The Ellison...
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...
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