technical manager
Responsibility
- providing clear guidance to investigators in relation to clinical specimen collection, process, storage, and handling
- identifying and working with vendors to deliver bioanalytical services in support of ongoing clinical development programs
- location : Strathclyde Business Park, Glasgow
Show more +13 - negotiating contracts and costings to deliver to business needs. Management of invoicing and approvals
- provide subject matter expertise in microbiology and scientific activities in relation to clinical development
- co-ordinating the design, implementation, and management of the technical and analytical aspects of clinical trial across multiple participating hospital sites, ensuring timely sample and data collection and Good Clinical Practice compliance
- development, maintenance and updates of technical and analytical study documentation and associated materials with the appropriate version controls
- liaising with bioanalytical providers to develop protocols and oversee activities to ensure data is reported accurately and in a timely manner for the responsible program
- providing supervision of more junior members of Clinical Operations staff, as required
- managing the co-ordination and oversight of the shipment of clinical trial samples and other supplies between EnteroBiotix, clinical sites and sample storage facilities
- support project team members to be compliant with current ethical and regulatory guidelines and requirements
- rewards and Benefits: Up to £60,000 ,flexible working, hybrid working, company bonus, share options, private healthcare, 33 days holiday, x4 life assurance, 5% pension contribution, enhanced parental leave, health and wellbeing allowance, healthy snacks, career progression and a dynamic culture
- intensively track and secure completion of actions by the responsible parties
- supervise the implementation of corrective action plans
- contributing to the management of clinical trials, working with the wider Clinical Operations team and clinical and regulatory contractors as part of a multidisciplinary research team
- contribute to clinical operations inspection readiness
Requirements
- clinical Research, Pharmaceutical or Biotechnology Industry.: 1 year
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