Senior Clinical Research Practitioner
7 months ago
The postholder will be responsible for discussing research opportunities with potential study participants, taking informed consent, planning and organising day to day research activities, collecting study data, collecting biological samples (including venepuncture and saliva samples), maintaining site files, liaising with study sponsors and the Research Office.
The post will require working with a wide range of people and working across teams; therefore, an excellent team orientated approach is essential as will excellent organisational and communication skills and an ability to plan and undertake work independently and efficiently.
MFT is England’s largest NHS Trust with a turnover of £2.5bn & is on a different scale than most other NHS Trusts. We’re creating an exceptional integrated health & social care system for the 1 million patients who rely on our services every year.
Bringing together 10 hospitals & community services from across Manchester, Trafford & beyond, we champion collaborative working & transformation, encouraging our 28,000 workforce to pursue their most ambitious goals. We set standards that other Trusts seek to emulate so you’ll benefit from a scale of opportunity that is nothing short of extraordinary.
We’ve also created a digitally enabled organisation to improve clinical quality, patient & staff experience, operational effectiveness & driving research and innovation through the introduction of Hive; our brand-new Electronic Patient Record system which we’ve launched in September 2022.
We’re proud to be a major academic Research Centre & Education provider, providing you with a robust infrastructure to encourage and facilitate high-quality research programmes. What’s more, we’re excited to be embarking on our new Green Plan which will set out how MFT continues to play its part in making healthcare more sustainable.
At MFT, we create and foster a culture of inclusion and belonging, provide equal opportunities for career development that are fair, open and transparent, protecting your health and wellbeing and shaping the future of our organisation together.
The postholder will be responsible for supporting research projects on the NIHR CRN genetics portfolio and other related studies at Manchester Centre for Genomic Medicine.
**Key duties include (but not limited to)**:
- To implement and carry out procedures to ensure the team is compliant with the principles of Good Clinical Practice, the Research Governance Framework and all regulatory legislation in their day-to-day practice.
- Obtain informed consent from participants for qualitative or non CTIMP trials as deemed appropriate and delegated to do so.
- Identify and recruit participants into clinical trials, assisting in the management, coordination and facilitation of the concurrent trials ensuring recruitment targets are met.
- Contribute to appropriate data collection and to monitor data in accordance with the research protocol and standard operating procedures.
- Maintain participant follow up in the form of telephone/ face to face contact for data collection ensuring study visit timescales are adhered to.
COVID-19 vaccination remains the best way to protect yourself, your family, your colleagues and of course patients from the virus when working in our healthcare settings. Whilst COVID-19 vaccination is not currently a condition of employment, we do encourage our staff to get vaccinated. If you are unvaccinated, there is helpful advice and information available by searching on the ‘NHS England’ website where you can also find out more about how to access the vaccination.
Diversity Matters
We’re looking forward to hearing from you
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