Sr Clinical Research Associate

United BioSource ,
London, Greater London
More Details

Overview

Job Description

UBC are looking for a CRA/SCRA with at least 2 years monitoring experience in the UK. You may be working on late phase studies, clinical trials or a combination of both. Ideally, we are looking for someone with experience in oncology and late phase studies but this is not essential. At UBC you will also be directly involved in site contract and budget negotiations. This is a great opportunity for a CRA from a large CRO background to gain new skills if you have no previous experience. Location is flexible -you can be office based in Hammersmith with the option for working from home 2 days per week - we will also consider home based if you live further afield. If you are looking to gain new skills and exposure to other phases with reduced travel, UBC may be just the place for you! Brief Description: Monitors in accordance with ICH, GCP, CFR guidelines, UBC and project SOPs Supervisory Responsibilities: Mentoring new and/or junior CRAs Requirements: * Bachelor's degree - Life Science preferred or equivalent years of industry and monitoring experience * At least 2 years active monitoring in the UK * Experience in electronic CTMS, EDC, eTMF * Minimum travel -approximately 20% depending on study allocation Specific Job Duties: * Thorough knowledge of UK legislation applicable to clinical trials/ observational studies and ICH GCP. * On site /remote monitoring visits * May be required to support/ mentor junior CRAs * Preparation, submission and tracking of local ethics committee and other regulatory applications * Contract and budget negotiation with hospitals and local R&D Departments * Study feasibility assessments where required #LI-CF1

People also viewed