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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...
Regulatory Affairs Coordinator
MARLOW
...experience ideally in clinical trials and CTR submission experience would be preferred. /p p strong Job Responsibilities include; /strong /p ul li a portfolio of CTAs including preparation and distribution of documentation associated with new initial CTAs and all CTA maintenance activities...
Regulatory Affairs Coordinator
MARLOW, SOUTH EAST ENGLAND
...experience ideally in clinical trials and CTR submission experience would be preferred. /p p br /p p b Job Responsibilities include; /b /p ul li a portfolio of CTAs including preparation and distribution of documentation associated with new initial CTAs and all CTA maintenance...
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EMEA Medical Affairs Director Hematology
HIGH WYCOMBE, BUCKINGHAMSHIRE, WYCOMBE, BUCKINGHAMSHIRE; BUCKINGHAMSHIRE; SOUTH EAST ENGLAND; ENGLAND, UK
...functional skills, Good Clinical Practice (GCP) and required SOPs is undertaken External Relationships Maintain and leverage relationships with investigators, EMEA thought leaders and patient groups to gain input into the development of the product strategy and to specific protocols As core MAP...
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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...
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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...
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 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...
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 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...
Consultancy Research Analyst
OXFORD, GB
...retrospective research, clinical trial feasibility. o Development of project proposals and pitch decks for the above. o Providing on-study analytic support for active recruitment projects. Work with sales and marketing team to develop our commercial pipeline of consultancy and clinical trial...
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...
Manufacturing Technician
OXFORDSHIRE, GB
...of prototypes, pre-clinical and clinical trial products for projects in ISO 8 cleanroom facility. Manufacturing batches to time and GMP standards. Cleaning and calibration of facilities equipment Cleaning and helping with monitoring of clean room facility Updating quality records and...
Director of Pharmacometrics
OXFORD, OXFORDSHIRE, OXFORDSHIRE; SOUTH EAST ENGLAND; ENGLAND, UK
...interventional clinical study, as well as to progress AI-designed small molecules into the clinical setting. Our pipeline demonstrates our ability to rapidly translate scientific concepts into precision-designed therapeutic candidates, with more than 15 projects underway. By designing...
Director / Senior Director, Project Management
WINDSOR, BERKSHIRE, WINDSOR & MAIDENHEAD, BERKSHIRE; BERKSHIRE; SOUTH EAST ENGLAND; ENGLAND, UK
Director / Senior Director, Project Management Precision for Medicine is a precision medicine CRO. Our uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical authorities, advanced biomarker and data...
principal data analyst (sas programming - pro/coa'sremote based - multiple locations globally
HORSHAM, WEST SUSSEX, WEST SUSSEX; SOUTH EAST ENGLAND; ENGLAND, UK
...knowledge of good clinical practices for data management is required to be successful Prepare, manage and analyse research data using standard statistical packages (e.g. SAS, S-Plus) Review project related documentations such as CRFs, SAPs and proposals and provide feedback to the project...
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...
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