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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, 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...
Principal Scientist- Molecular Pharmacology
£45000 - £60000/annum
BERKSHIRE
...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...
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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...
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...
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Regulatory Specialist
MAIDENHEAD, ENGLAND, UNITED KINGDOM
...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...
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...
Lead Principal Scientist - Drug Discovery
48445
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...
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...
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 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...
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Nurse Assessor
£44800/annum
WITNEY, OXFORDSHIRE, OX28
...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? RGNs look no further My client is seeking an enthusiastic and energetic RGN to...
Registered Nurse
£40533/annum
WATERLOOVILLE, HAMPSHIRE, PO7
...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...
Scientist
KENT, GB
Description: We are working alongside a leading Pre-Clinical CRO specialising in Neuroscience to a hire a Scientist / Senior Scientist for their site in Sandwich, Kent. Who we are: We are a dynamic recruitment agency that has evolved since our first establishment in 2012. We work with several...
Associate Director, Clinical Pharmacology
SURREY, UNITED KINGDOM
...The Associate Director, Clinical Pharmacology is responsible for leading clinical research activities with focus on clinical pharmacology phase I pharmacokinetics and bioequivalence trials. He/she will ensure that high quality expertise is provided to meet state-of-the-art scientific, industry and...
Experienced Senior Research Nurse
LONDON, SOUTH EAST ENGLAND
Experienced Senior Research Nurses Phase 1 & 2 clinical trials p b Starting salary £41,800–£48,650 /b /p p + estimated £3,000 for unsocial hours shifts /p p /p p We are looking for experienced Senior Research Nurses to help lead the clinical...
Scientist
KENT, SOUTH EAST ENGLAND
p Description: /p p We are working alongside a leading Pre-Clinical CRO specialising in Neuroscience to a hire a Scientist / Senior Scientist for their site in Sandwich, Kent. /p p br /p p Who we are: /p p We are a dynamic recruitment agency that has evolved since our first establishment in...
Senior Scientist - Imaging
LONDON, SOUTH EAST ENGLAND
...and report on pre-clinical discovery research studies across various therapeutic areas. /li li Utilise and expand on your scientific domain expertise, offering expertise and leadership to the wider team. /li li Lead communications with sponsors: understanding needs, presenting study...
Associate Director, Clinical Pharmacology
SURREY, SOUTH EAST ENGLAND
...The Associate Director, Clinical Pharmacology is responsible for leading clinical research activities with focus on clinical pharmacology phase I pharmacokinetics and bioequivalence trials. He/she will ensure that high quality expertise is provided to meet state-of-the-art scientific, industry and...
Associate Director, Clinical Pharmacology
SURREY, ENGLAND
...The Associate Director, Clinical Pharmacology is responsible for leading clinical research activities with focus on clinical pharmacology phase I pharmacokinetics and bioequivalence trials. He/she will ensure that high quality expertise is provided to meet state-of-the-art scientific, industry and...
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