| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| Oil & Gas Jobs |
| Banking Jobs |
| Construction Jobs |
| Top Management Jobs |
| IT - Software Jobs |
| Medical Healthcare Jobs |
| Purchase / Logistics Jobs |
| Sales |
| Ajax Jobs |
| Designing Jobs |
| ASP .NET Jobs |
| Java Jobs |
| MySQL Jobs |
| Sap hr Jobs |
| Software Testing Jobs |
| Html Jobs |
| Job Location | West Lothian |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
Are you an experienced Clinical Research Associate looking for a new exciting job opportunityWe are currently looking for a Clinical Research Associate to join a leading life sciences company based in the Central Belt of Scotland with the possibility of home working.As the Clinical Research Associate you will be responsible for the coordination of a variety of clinical trials in oncology and viral (cell immunotherapy) to ensure that trials are conducted in accordance with ICH GCP and other relevant regulatory guidelines, protecting the safety of participants and the quality of the data.KEY DUTIES AND RESPONSIBILITIES:Your duties as the Clinical Research Associate will be varied however the key duties and responsibilities are as follows:1. You will take ownership of assigned studies and carry out site selection/feasibility, support to EC/RA submissions, initiations, on-site monitoring, and close-out activities.2. You will be responsible for ensuring appropriate attention is provided to the sites in order to drive data quality so that the clinical study protocol requirements are fulfilled within the appropriate regulatory and ethical framework.3. As the CRA, you will be establishing regular lines of communication plus administering protocol and related study training to assigned site as well as manage multiple priorities across various clinical trials.4. Additionally, you will manage the clinical trial progress by tracking regulatory submissions, recruitment, case report form (CRF) completion and data query resolution.ROLE REQUIREMENTS:To be successful in your application to this exciting opportunity as the Clinical Research Associate we are looking to identify the following on your profile and past history:1. A Bachelors degree in a health care or other scientific discipline as well as experience in monitoring as CRA within Oncology or Viral is essential for this position.2. You will also need to have thorough knowledge of ICH GCP and other industry recognised standards and guidelines as well as conducting clinical trials in general. 3. Experience in site set up and regulatory and EX submissions in EU and US would be advantageous. Any experience in haematology, immunotherapy and/or cell therapy would also be beneficial.Key Words: Clinical Research Associate | Clinical Studies | Clinical Trials | GCP | Regulatory | Immunotherapy | Viral | Oncology | Cancer Research | Life Science Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.