Offres clinical trials à Richmond

Ensure that all the required approvals are acquired and maintained in order to support clinical trials for investigational medicinal products as well as to market approved medicinal products

IXI), is a leading neuroimaging Contract Research Organization (CRO), delivering advanced Ai analytical insights in neuroscience to the global clinical trials market. Established in 2004, listed as a ...

Research Trials continue to showcase the therapeutic potential of psychedelic pharmacotherapies ... Wenham Carter Search Firm are partnered with a growing Clinical Research Organization, who are ...

Coordinate submission strategies for global clinical trials, ensuring alignment with regulatory strategies, and promptly highlighting any risks or issues to GRPT and study teams * Ensure timely ...

Ensure the 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 ...

In this role you be responsible ensuring precision, dependability, and thoroughness of Phase I-IV clinical databases, overseeing all data management tasks throughout designated trials. You will ...

Proclinical are seeking a dedicated Snr Clinical Trial/ Program Manager to accelerate the initiation and execution of Advanced Therapy Medicinal Products (ATMPs) clinical trials within one of our ...

In this position you will contribute to the development of compounds within the oncology therapeutic area and drive the design of innovative and efficient clinical trials. As the Head of ...

Clinical Research Organisations, advisors, vendors), to support the seamless and timely delivery of clinical trials. The CTOS is accountable for supporting the oversight of trial supplies ...

... clinical ... trials. Responsibilities: • Oversee a portfolio of CTAs, managing the preparation and ...

Current awareness/experience of clinical trials and a passion for the underlying science. * Proficiency in Microsoft Office tools. * Intermediate knowledge of Excel, including Graphing, Vlookup, and ...

As a Regulatory Affairs Professional, you will assume a crucial role in providing leadership and expertise in all regulatory and submission-related aspects of clinical trials. You will serve as the ...

Manage strategy and execution for all regulatory CMC submissions (e.g. late stage clinical trials, variations, extensions and marketing applications). * Author and coordinate responses to questions ...

My client are looking for a highly motivated Senior Project Manager to manage the conduct of post-authorisation studies and interventional clinical trials in accordance with protocols, GxP guidelines ...

General clinical trials experience/deep understanding. Up to 2 years of experience in CRA IVD role preferred but not required. Must be able to travel within UK and EU region on occasion. EDUCATION ...

Strategically evaluate and commercialise data products suitable for clinical trials. * Navigate complex market and regulatory landscapes to identify and partner on emerging opportunities. * Lead ...

- Accountable for attracting, planning, execution and monitoring of clinical trials through all phases (from feasibility to close-out) in conformance to ICH-GCP, relevant SOPs, other procedural ...

Manages strategy and execution for all regulatory CMC submissions (e.g. late stage clinical trials, variations, extensions and marketing applications) for products within the portfolio in compliance ...

Acting liaison and support for Immunomonitoring and R&D labs, assisting in quality assurance aspects of the company's Clinical Trials * Act as the system administrator for the eQMS, write and/or ...

To ensure that the client acquires and maintains all the required approvals in order to support clinical trials for investigational medicinal products as well as to market approved medicinal products

... clinical trials in neuroradiology. 💼 Professional Development Opportunities: Our client prioritises investing in the professional growth and development of its staff. As a Consultant ...

Features include: monthly workshops, courses, skills training, a peer to peer connect service, a national clinical trials finder, a library of shared resources and much more. The Academy is currently ...

Experienced Senior Research Nurses Phase 1 & 2 clinical trials Starting salary £41,800-£48,650 + estimated £3,000 for unsocial hours shifts We are looking for experienced Senior Research Nurses to ...

Title: Clinical Trial Manager - Global Pharma - Complex Trials. Thorough knowledge and understanding of FDA and EU Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable. We’re very excited to be partnering with a Global Pharma who are seeking a Clinical Trial...