23/04/2024 | Fulltime | British Heart FoundationOne in four people in the UK. That is why we need you. About the role As our Senior Research Advisor for Clinical Fellowships, youll be responsible for the scientific management of BHFs diverse portfolio of personal funding awards, which range from PhD studentships through to Senior Fellowships
Save for later20/04/2024 | Fulltime | Novartis Pharma GmbHSenior Clinical Data Scientist (Trial Data Manager) Job ID 394976BR Apr 19, 2024 Vereinigtes Königreich About the Role 100,000+ That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global Clinical Operations, redesigned to enable faster trial
Save for later10/04/2024 | Fulltime | CV-Library | - £40 / Hour Clinical Safety Scientist to join a company in the pharmaceutical industry at their site based in Brentford on a contract basis for 12 months. Salary Up to £40.00 per hour PAYE. This role is inside IR35. Clinical Safety Scientist Role Assisting with the monitoring & evaluation of safety profiles
Save for laterRegister your CV20/04/2024 | Fulltime | Our Future Health LimitedAnd scientists, bringing your expertise to ensure that the team is successful. In this role your key responsibilities will include but not be limited to - Working in cross-functional teams that are creating and launching new data-driven products. - Hands-on development of new data features tailored to clinical
Save for later19/04/2024 | Fulltime | Pfizer BelgiumThe development and management of clinical protocols and amendments, investigator brochures, and clinical study reports Provideleadership to medical directors and clinical scientists who lead the clinical study teams Oversee the evaluation of safety, pharmacology, and efficacy data from ongoing and completed
Save for later18/04/2024 | Fulltime | Pharma SearchAre you passionate about advancing Oncology clinical development? Would you relish the challenge of working within a leading global organization; one where you will enjoy a high level of responsibility and autonomy, whilst able to focus on further enhancing your therapeutic expertise? Our client
Save for later18/04/2024 | Fulltime | Hobson Prior International LtdAnd potentially reportable cases such as SUSARs/INDSRs. - Maintain close communication with clinical development physicians to ensure availability of essential safety, clinical, and laboratory data. - Participate in monthly Safety Management Team meetings led by clinical development. - Chair Safety Review Teams
Save for later15/04/2024 | Fulltime | Deep Science Ventures LimitedWith a focus on tumour biology, immunology and pre-clinical development. In addition, you will be teamed up with our Venture Partner for this opportunity, Dr. Stevel Powellalongside a growing scientific advisory board. THE OPPORTUNITY AREA Immunotherapies, especially antibody-based immune checkpoint
Save for later14/04/2024 | Fulltime | Hobson Prior International LtdSupervise or prepare chemicals, reagents, solutions, and process samples generated in a clinical study as per Standard Operating Procedures (SOPs) and Working Instructions. - Perform or supervise the processing of samples using Immunoassay techniques and commercially available quantification software, e.g
Save for later14/04/2024 | Fulltime | Barrington James LimitedWill serve as an integral member of the due diligence and licensing team, spearheading the evaluation of assets, in-licensing prospects, and other business intelligence and development opportunities. Responsibilities 1. Actively engage in the scientific, clinical, and commercial evaluation of oncology
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