Overview
In this role you support and lead clinical research across the Trust, with responsibility for trial setup, delivery and safety in line with regulations. You will work within a multidisciplinary team to provide medical cover, conduct studies to Good Clinical Practice, and oversee regulatory documentation and records. You will collaborate with the R&D department and RDN to achieve the Trust’s research goals and ensure studies meet targets. This is a patient-focused opportunity in a mission-driven NHS environment that values inclusion and advancement in research.
Responsibilities
- Act as principal or sub-investigator for clinical research studies, providing medical cover and ensuring safety, timeliness and target delivery
- Lead or participate in trial setup, conduct, and management in accordance with regulatory requirements and GCP
- Maintain accurate regulatory and study records (paper and electronic) as required by authorities and sponsors
- Engage with the R&D department and local Research Delivery Network (RDN) to support organisational research targets
- Identify suitable studies and assist with sponsor applications on behalf of the Trust
- Provide medically informed decisions within their expertise, in consultation with Principal Investigators
- Foster relationships across Trust departments to aid smooth study setup and operation
Key requirements
- Completion of core speciality training or equivalent
- Full GMC registration and a licence to practise
- Significant practical experience of research delivery
- Desirable: Experience in audit
- Desirable: Experience of leadership within a research setting
- Essential Qualifications: MBBS or equivalent
- Desirable: MRCP (UK) or equivalent; BSc or intercalated degree
- Excellent communication with patients and carers
- Ability to prioritise tasks
- Strong interpersonal and collaborative skills
- Proven ability to manage acute medical emergencies
- ALS provider
- Proficient with computers and adaptable to new platforms
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