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Registered Nurse
WITNEY
...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 furtherMy client is seeking an enthusiastic and energetic registered...
Registered Nurse
WITNEY, SOUTH EAST ENGLAND
...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 furtherMy client is seeking an enthusiastic and energetic registered...
Registered Nurse
WITNEY, UNITED KINGDOM
...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 furtherMy client is seeking an enthusiastic and energetic registered...
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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...
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...
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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...
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...
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...
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...
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...
Scientist
KENT
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 br Read the overview of this opportunity to understand what skills, including and relevant soft skills 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...
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...
Principal Scientist
READING, SOUTH EAST ENGLAND
...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 br /p p To be considered for the role you will you will ideally hold a PhD in...
Senior/Principal Scientist
READING, SOUTH EAST ENGLAND
...within In-Vitro Pharmacology - preferably with significant antibody discovery experience. /p p br /p p Responsibilities: /p p br /p ul li Implement pharmacological and immunological assays in order to characterise antibody candidates /li li Motivate and lead project 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...
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...
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