Job offers for Research Manager Medical jobs in Dundee

15/05/2024 | Fulltime | Dundee | CV-LibrarySimultaneously in a fast-paced environment. ·Sound judgment and decision-making skills, with a keen attention to detail and a commitment to upholding ethical standards. Benefits ·Competitive salary commensurate with experience. ·33 days holiday allowance ·Private medical insurance ·Company Car Allowance

07/05/2024 | Fulltime | Dundee | CV-Library | Customer and client engagement - Property and Estates Management - Corporate and/or charity governance - Medical research The successful candidate will demonstrate a strong and visible passion and commitment to Sight Scotland and Sight Scotland Veterans, its strategic objectives and mission

01/05/2024 | Fulltime | Dundee | CV-LibraryA comprehensive programme of learning and development. - Competitive base salary. - 25 days annual leave, with the opportunity to buy more. You’ll even get your birthday off as well! - Private medical insurance. - Life assurance 4x salary. - Enhanced pension with up to 8.5% employer contributions. - A huge range

01/05/2024 | Fulltime | Dundee | CV-Library | £42,700 - £47,000 / Year The culmination of the device risk management program through the final risk benefit analysis. - Contribute to early-stage development and risk assessments and assess Risk Management files through the routine review program as required, including monitoring of the competitor landscape and review of medical device

25/04/2024 | Fulltime | Dundee | CV-Library | £45,000 / Year Health of life science field. - Proven clinical trial experience, clinical trial management; CRO experience preferred. - Experience in Phase I-IV trials; Phase II - III is preferred. - Working knowledge of EU Clinical Trials Directive, Medical Device Directive, UK Clinical Trials Regulations, Principles

15/04/2024 | Fulltime | Dundee | CV-Library | £30,000 / Year Directive, Medical Device Directive, UK Clinical Trials Regulations, Principles of ICH-GCP, GDPR and Research Governance Framework Legislation with proven ability to apply these to the coordination of clinical trials. - Understanding of current EU Medical Device Regulation. - Working knowledge of BS EN ISO