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Clinical Research Fellow

3 months ago


Runcorn, United Kingdom Warrington and Halton Teaching Hospitals NHSFT Full time

Job summary

The Clinical Research Fellow (CRF) will join a multi-disciplinary, collaborative and award-winning R&D Team. The role's main base is the Halton Clinical Research Unit (HCRU), a former ward converted into dedicated research space. The role will provide the daily medical leadership and with responsibility for clinical studies conducted on the unit.

As a Clinical Research Fellow, your responsibilities include the safety of participants, ensuring quality data collection which is accurate and timely, supporting the development of sustainable research capacity across the Trust and improving the reputation of the unit through strategic planning and delivery to time and target. The role is also expected to engage with professional or industry networks, support research partnerships or collaborations, attend relevant industry conferences and meetings, and participate in awareness raising programmes and events.

Due to the nature of the role, the postholder should be comfortable working autonomously with remote supervision. They should also have excellent communication skills, both with staff and participants.

Main duties of the job

The CRF is expected to take a proactive approach to managing the trials hosted on the HCRU. They will be deeply involved with securing the clinical trial pipeline, assessing feasibility and formulating recruitment strategies, delivery to time and target, and safety reporting. The post-holder must be able to carry out trial protocols and local policies and procedures to a high standard.

You should have significant experience and trial delivery, including knowledge of all relevant legislation, regulatory frameworks and compliance, and local, regional and national policies affecting the research landscape.

The CRF is responsible for the safety of participants on the HCRU. This includes ensuring procedures for fully informed consent, maintaining high standards of communication with participants. You will also be responsible for ensuring that data collected from participants is complete and accurate.

About us

Warrington and Halton Teaching Hospitals NHS Foundation Trust is a caring and compassionate organisation that is both ambitious and innovative. We are committed to delivering the best outcomes for our patients and providing a positive experience of our staff. We aspire to be outstanding for our patients, our communities and our staff and are committed to being a great place to receive healthcare, work and learn.

Straddling the neighbouring boroughs of Warrington and Halton we are part of the Cheshire and Merseyside Integrated Care system. Our hospitals are ideally situated to meet the growing healthcare needs of the 330,000 population of these boroughs.

Warrington Hospital is home to our emergency, critical care and maternity services, Halton Hospital is focused on elective procedures and the Runcorn Urgent Treatment Centre, although many services are offered at both sites and in community hubs.

A CQC-rated 'good' organisation with 'outstanding' features, we are working towards university hospital status, having achieved teaching hospital status in 2019.

Our workforce of nearly 5,000 across both sites comprises more than 50 nationalities. We strive to be an equal, diverse and inclusive employer, which is recognised as a pioneer in its equality, diversity and inclusion work. The Trust is proud to have achieved numerous external accreditations and is working towards achieving the Anti-Racist Organisation Framework, recognising the importance of anti-racism in all that we do.

Job description

Job responsibilities

The main duties and responsibilities of the role include, but are not limited to:

Medical leadership for clinical trials on the HCRU and support for the wider portfolio Ensure compliance with protocol, policy and regulation (such as the ICH-GCP, Human Tissues Act and Data Protection Act) Prompt safety reporting Ensuring consents are fully informed Capacity assessments High quality communication with study teams/Sponsor representatives Conduct physical examinations and procedures as required by protocol Clinical review of physical examinations and test results Onward referral to appropriate health service if required Maintain professional training and certifications Ensure that local policies are adapted to protocols where required Close liaison with Pharmacy Clinical Trials team Maintain inspection readiness Support and develop the research capacity across the Trust and across the boroughs of Warrington and Halton, including working with external organisations Support the visibility and quality of R&D's reputation for timely and quality delivery of clinical trials Strengthen the pipeline of commercial clinical trials coming into WHH Training, development and raising awareness of research across the Trust - mainly medical and NMAHPs but may be any staff groups Undertake audits, quality assurance, quality improvement or service evaluations if directed to do so Proactive identification of opportunities for the above

Please see job description or contact the Lead Recruiter for further details.

Person Specification

Qualifications

Essential

MBChB/MBBS or equivalent Full registration with GMS Valid ALS certification

Desirable

Additional higher degree in relevant field Undergraduate awards and prizes Postgraduate clinical qualification (MRCP (UK) or equivalent)

Experience

Essential

Significant practical experience of research delivery At least 24 months of clinical experience post qualification

Desirable

Experience in clinical audit Experience in delivery of clinical trials in commercial life sciences

Skills

Essential

Ability to manage acute medical emergencies Ability to prioritise tasks Excellent communication skills with patients, carers and colleagues Insight into own abilities and experience

Desirable

Current GCP certificate (issued within the last 2 years) Presentations of posters or abstracts and local, regional or national meetings Publications in peer-reviewed journals

Specific Role Requirements

Essential

Able to show initiative and work independently Demonstrates behaviours that meet Trust values Demonstrates commitment to continued medical education

Desirable

Experience of teaching at undergraduate or post-graduate level