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Research Midwife - 18 mths
| Posting date: | 17 April 2025 |
|---|---|
| Salary: | £37,338.00 to £44,962.00 per year |
| Additional salary information: | £37338.00 - £44962.00 a year |
| Hours: | Full time |
| Closing date: | 01 May 2025 |
| Location: | Bradford, BD9 6RJ |
| Company: | NHS Jobs |
| Job type: | Contract |
| Job reference: | C9389-25-0350 |
Summary
Research Identify potential study participants and undertake the co-ordination of trial screening procedures to assess patient suitability, undertake accurate data collection, collation and recording of data. Recruit eligible participants to studies by ensuring that they and their families (where appropriate) are fully informed of all treatments and procedures to facilitate effective, informed consent. Assess trial participants using specific pre- determined protocols. Contribute to team research projects, working alongside the team research fellow. Act as participant's advocate. Accurately report and document adverse events. Provide on-going support and information to the patients and their families. Ensure adherence to all relevant data protection regulations. Collect, process and dispatch biological trial samples according to trial protocols and Trust policies and guidelines. Clinical To safeguard patient interest by liaison with relevant clinical trial personnel, ensuring compliance with ICH GCP Guidelines. ensure compliance with NMC Code for clinical competence and statutory learning. Professional Work within the NMC Code of Conduct and scope of professional conduct. Exercise personal accountability for own practice and ensure any changes are achieved within scope of professional practice. Adheres to all Trust Policies and Procedures. Work as part of multidisciplinary team and contribute to the on-going development of the department. Be responsible for maintaining strong relationships and positive communication channels with other key personnel. Be responsible for sustaining own knowledge, clinical skills and professional awareness in accordance with NMC Code and Revalidation requirements. Attend management and service meetings. Work alongside Research and Development department as required. Ensure that the trial is conducted to the standards required by ICH/GCP, the EU Directive and any other relevant regulations. Ensure all proposed research projects carried out are registered and reviewed by the trust Research and Development department (R&D) and Research Ethics Committee (REC) prior to commencement and that updates and amendments are reported in a timely fashion. Take an active approach in the promotion of research awareness, developing skills in self and others. Attend local and national courses on Research Governance as appropriate and maintain up to date training in ICH/GCP. Keep up to date with current developments relevant to the care of research participants in the clinical trial. Administrative Ensure up to date and approved protocols and participant information is available. Accurately collate data on relevant trial proformas within a pre-determined time frame and respond to data queries. Accurately and promptly report serious adverse events to relevant authority. Prepare and present data when requested by appropriate authority. Ensure the safe storage of research and patient documentation that is clearly traceable. Assist with maintaining databases of clinical trial activity, including recruitment and screened participants. Education and training Ensure Trust clinical and information governance regulations are adhered to. Attend national trial meetings and feed back to the research team and wider clinical team. Within the framework of clinical governance, work continuously to improve quality and safeguard standards of care. Help identify any gaps in evidence base. To have in depth knowledge and understanding of trial protocols. Develop an understanding of different research methodologies. Maintain an environment that is conducive to learning. Actively participate in the development of own personal development plan and performance review.