
BRC MND Project Coordinator
- Sheffield
- £38,682-46,580 per year
- Contract
- Full-time
- Educated to degree level in Health/ Biomedical Sciences/ Neuroscience related subject or equivalent experience in a clinical research environment.
- Project Management qualification or demonstrable equivalent experience.
- Current GCP accreditation
- MSc in Health related/ Biomedical Science/ Neuroscience related subject
- Extensive experience of clinical research in the NHS, Academic or commercial environment.
- Experience of project design, management and evaluation.
- Experience of the submission and approval process for set up of clinical trials.
- Extensive experience managing clinical research performance metrics.
- Experience of co-ordinating multiple projects at any one time.
- Experience of working independently and as part of a team.
- Experience of working collaboratively with internal and external partners.
- Experience of working in a fast paced, adaptable environment.
- Experience of process innovation and other service improvement initiatives. Experience of developing Standard Operating Procedures, Policies and Procedures.
- Experience with lab based kits and consumables
- Knowledge of research processes and research methods applicable to health setting
- Knowledge of Department of Health & Social Care/NIHR research strategy
- Knowledge of research legislation including research governance, ICH GCP, Medicines for Human use (Clinical Trials) Regulations, Data Protection, Human Tissue Act, Mental Capacity Act.
- Knowledge of the national research agenda for NIHR Biomedical Research Centres
- Knowledge of patient and public involvement initiatives.
- Knowledge, experience and maintenance of quality assurance systems.
- Ability to maintain timely, highly complex and accurate information sources and databases.
- Excellent organisational skills and an ability to prioritise an unpredictable workload with frequent disruption
- Understanding and commitment to the need for confidentiality.
- Knowledge of research funding sources, especially NIHR.
- Ability to manage a diverse workload and to meet set deadlines on own initiative and without close supervision.
- Ability to work independently, without supervision and to self-motivate.
- Ability to produce high quality performance reports for various stakeholders.
- Demonstrable self-awareness, an understanding of impact on others and an ability to manage self and maintain professional conduct in difficult and challenging situations.
- Extensive experience of PC applications such as Excel, Word, PowerPoint, Microsoft Project Manager and Access, using skills at an advanced level of expertise.
- Excellent attention to detail, whilst maintaining the ability to see the bigger picture.
- Proactive in fulfilling needs of researchers.
- Ability to analyse and communicate to the BRC Operational Group and Executive Committee complex data from various sources to enable continuous quality and delivery efficiencies.
- Evidence of report writing and presentation skills.
- Educated to degree level in Health/ Biomedical Sciences/ Neuroscience related subject or equivalent experience in a clinical research environment.
- Project Management qualification or demonstrable equivalent experience.
- Current GCP accreditation
- MSc in Health related/ Biomedical Science/ Neuroscience related subject
- Extensive experience of clinical research in the NHS, Academic or commercial environment.
- Experience of project design, management and evaluation.
- Experience of the submission and approval process for set up of clinical trials.
- Extensive experience managing clinical research performance metrics.
- Experience of co-ordinating multiple projects at any one time.
- Experience of working independently and as part of a team.
- Experience of working collaboratively with internal and external partners.
- Experience of working in a fast paced, adaptable environment.
- Experience of process innovation and other service improvement initiatives. Experience of developing Standard Operating Procedures, Policies and Procedures.
- Experience with lab based kits and consumables
- Knowledge of research processes and research methods applicable to health setting
- Knowledge of Department of Health & Social Care/NIHR research strategy
- Knowledge of research legislation including research governance, ICH GCP, Medicines for Human use (Clinical Trials) Regulations, Data Protection, Human Tissue Act, Mental Capacity Act.
- Knowledge of the national research agenda for NIHR Biomedical Research Centres
- Knowledge of patient and public involvement initiatives.
- Knowledge, experience and maintenance of quality assurance systems.
- Ability to maintain timely, highly complex and accurate information sources and databases.
- Excellent organisational skills and an ability to prioritise an unpredictable workload with frequent disruption
- Understanding and commitment to the need for confidentiality.
- Knowledge of research funding sources, especially NIHR.
- Ability to manage a diverse workload and to meet set deadlines on own initiative and without close supervision.
- Ability to work independently, without supervision and to self-motivate.
- Ability to produce high quality performance reports for various stakeholders.
- Demonstrable self-awareness, an understanding of impact on others and an ability to manage self and maintain professional conduct in difficult and challenging situations.
- Extensive experience of PC applications such as Excel, Word, PowerPoint, Microsoft Project Manager and Access, using skills at an advanced level of expertise.
- Excellent attention to detail, whilst maintaining the ability to see the bigger picture.
- Proactive in fulfilling needs of researchers.
- Ability to analyse and communicate to the BRC Operational Group and Executive Committee complex data from various sources to enable continuous quality and delivery efficiencies.
- Evidence of report writing and presentation skills.