WORKING RELATIONSHIPS: Accountable to the New Drug Development and Scientific Affairs Manager on a day to day basis. DUTIES AND RESPONSIBILITIES (NOT LIMITED) Clinical trial officer is responsible for the co-ordination, tracking and documentation of clinical trial activities. The CTO will also provide support for the preparation and filing of trial related communications and docume...
Cell Culture Technician Evidence of a Hepatitis B vaccination is ESSENTIAL for this role. The Role: A new opportunity has arisen where our client is seeking a Cell Culture Technician located in their London site. The main focus of this role will be to work within the cell culture lab within the translational research team and maintain both the laboratory and the cell lines used in translational researc...
Job Summary Provides customer-focused leadership in the execution of the start up of sites in one or multiple Phase II through Phase IV clinical trials across all functional Site Start-Up (SSU) areas. Accountable for the delivery of activation-ready study sites on time, on budget, and in compliance with all applicable regulations. Responsible for managing all site start-up activities from site selection/recommendation thru site-...
Job Summary Our General Medicine Business Unit is hiring INC Research specializes in providing clinical trials services to support global Phase I - Phase IV studies, and we offer deep therapeutic clinical trial expertise across a wide variety of indications, as well as for special populations, such as women and pediatrics. Core Responsibilities We are currently loo...
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Date: 6 days ago
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City Of London, London
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£40,000 - £50,000 per annum, negotiable, pro-rata, inc benefits, OTE
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3 applications
Head of Clinical Trial Supply CRO In parallel to the commercial roll out of key productfor patients with Multiple Sclerosis, the company is continuing phase three clinical trials in patients with advanced cancer. A number of trials are planned for countries across the world; therefore we are looking to appoint a hands-on Head of Clinical Trial Supplies to provide leadership in the execution of this programme. Reporting to ...
The Role: A fantastic permanent opportunity has become available at a leading CRO based in central London for a QC Manager. To ensure you are successful within this role your crucial tasks will include, taking responsibility for all elements of QC documentation and data produced by the various project teams, from the screening and quarantine to the follow up phases of the trials. You will also need to ensue all elements of documentatio...
Job Description: We are assisting our client in finding a Senior Specialist for their Phase I unit in North West London. The post holder will provide guidance on requirements for the conduct of clinical trials including: • Maintain drug accountability records in accordance with agreed protocols and the principles of International Conference on Harmonization Good Clinical Practice (GCP) and Good Manufacturing Practice (...
We are assisting our client, a medical communications agency, in finding a (senior) medical writer to be based in Cheshire or London. There will be a full & varied workload, including publications-related work, meetings (advisory boards, symposia, masterclasses), multi-media deliverables, etc. Key objectives • To consistently produce high quality medical education & communications materials for the pharmaceutic...
Pharmacetical company in SE England is seeking a Head of Clinical Trial Supplies. Responsibilities: Reporting to the Supply Chain Director the successful candidate in this newly created position will lead a team of staff undertaking the control, administration, labelling, packaging, despatch and returns of investigational medicinal products (IMP). In this responsible position you will b...
Job Description: Our client is looking for a Regulatory Compliance Administrator to be based in South West London. The company is involved in Phase I-IV research trials including pharmacokinetic studies in patients, and healthy volunteer studies. The Regulatory Compliance Administrator is responsible for assisting the Head of Regulatory Compliance and Regulatory Compliance Coordinator in all aspects of Regulator...
