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We've expanded the search to "Hampshire" to find more jobs with all your keywords
Registered Nurse
£40533/annum
HEDGE END, HAMPSHIRE
...your medical and pharmacology knowledge? Are you seeking a role where your work-life balance is important to your organisation? Do you want your efforts rewarded? CPD paid for? Training and development given? RNs look no further My client is seeking an enthusiastic and energetic registered...
We've expanded the search to "South East" to find more jobs with all your keywords
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...
Lead Principal Scientist - Drug Discovery
£50,000+ per annum , GBP
BERKSHIRE
...validation through to clinical development. Innovate and apply the latest methodologies and technologies to enhance the drug discovery and development process. Leading and contributing to the development of novel therapeutic antibodies and biologics targeting critical disease pathways. Present...
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Principal Scientist
READING, GB
...target validation and clinical development. You will also work cross-functionally with wider teams as well as look to present and deliver findings to key stakeholders through presentations and publications. To be considered for the role you will you will ideally hold a PhD in Molecular Biology...
Senior/Principal Scientist
READING, GB
...within In-Vitro Pharmacology - preferably with significant antibody discovery experience. Responsibilities: Implement pharmacological and immunological assays in order to characterise antibody candidates Motivate and lead project and laboratory teams Present findings to internal...
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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...
Principal Scientist, Preformulation and Biopharmaceutics
SITTINGBOURNE, UNITED KINGDOM
...the optimization of pre-clinical and clinical formulations through rational experimental design, thoughtful execution, and clear data interpretation. Carry out solubility and dissolution experiment to assess the stability and predict the bio-performance of our internal formulations. Identify gaps...
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...
Senior/Principal Scientist
READING
...within In-Vitro Pharmacology - preferably with significant antibody discovery experience. /p p Responsibilities: /p ul li Implement pharmacological and immunological assays in order to characterise antibody candidates /li li Motivate and lead project and laboratory teams /li li...
Principal Scientist
READING
...target validation and clinical development. You will also work cross-functionally with wider teams as well as look to present and deliver findings to key stakeholders through presentations and publications. /p p To be considered for the role you will you will ideally hold a PhD in Molecular...
Senior Scientist
46875
READING
...within In-Vitro Pharmacology - preferably with significant antibody discovery experience. Responsibilities: Implement pharmacological and immunological assays in order to characterise antibody candidates. Motivate and lead project and laboratory teams. Present findings to internal...
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...
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...
Principal Scientist - Molecular Biology
48629
BERKSHIRE
...target validation to clinical development. Foster a culture of scientific rigor and innovation. Stay up to date with emerging technologies and advancements applicable to the field of in-vitro assay development. Present project updates and findings to stakeholders and collaborators and...
Senior Scientist
£50000 - £60000/annum
READING, BERKSHIRE, RG1
...target validation and clinical development. You will also work cross-functionally with wider teams as well as look to present and deliver findings to key stakeholders through presentations and publications. To be considered for the role you will you will ideally hold a PhD in Molecular Biology...
Paramedic
£44800/annum
DARTFORD, KENT, DA1
...your medical and pharmacology knowledge? Are you seeking a role where your work-life balance is important to your organisation? Do you want your efforts rewarded? CPD paid for? Training and development given? Look no further My client is seeking an enthusiastic and energetic registered...
Principal Scientist- Molecular Pharmacology
BERKSHIRE, UNITED KINGDOM
...development, molecular pharmacology, and cell biology. As a Principal Scientist, you must also have a strong leadership background.Key Responsibilities:Implement cutting-edge pharmacological and immunological assays to characterize antibody candidates and assess their therapeutic potential...
Regulatory Manager, Clinical Trial Strategy & Submissions
MAIDENHEAD, 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...
Lead Toxicologist
38277
READING, BERKSHIRE, RG1
...studies to support clinical trials and product registration for BCH s global market Produce documents for Health Authorities for non-clinical purposes, e.g. CTD nonclinical modules and justification documents, with minimal guidance and supervision Generate biocompatibility risk...
We've expanded the search to "England" to find more jobs with all your keywords
Senior Health Outcomes Researcher
CITY OF LONDON, GB
...literature reviews of clinical, health economic, and real-world evidence. These reviews often inform manuscripts or health technology assessment materials and can lead to qualitative or quantitative synthesis. Responsibilities: - Run systematic reviews and carry out evidence synthesis using...
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