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  • Job
    Full-time
    Entry & Junior Level
  • Research & Development
    Healthcare

AI generated summary

  • You must work with consultants, have clinical skills like phlebotomy, be IT proficient, interact with patients, and lead studies with training. A structured induction and mentorship are provided.
  • You will support patient recruitment, interact with patients, manage data entry, maintain study documentation, process amendments, and lead an observational/genetic study post-training.

Requirements

  • The successful candidate will work with specialist consultants and clinical trial units.
  • There is the potential for the successful candidate to utilise and develop existing clinical skills to support the Research Midwives/Nurses such as phlebotomy and vital signs collection.
  • The role also has a significant administrative element and a requirement to be IT proficient and able to accurately capture research data from patients and their medical records.
  • You will be expected to interact with patients & families in relation to the requirements of clinical trials & be able to work without supervision in some areas.
  • There will be a requirement to lead an observational/genetic study following appropriate training & mentorship.
  • This is an excellent opportunity for anyone who wishes to develop skills & expertise in research and to develop our Trust's research portfolio.
  • We are one of the few NHS organisations recognised as an ‘investor in people’ and works to involve support and develop staff within the organisation, alongside one culture of care.
  • There will be a structured induction, training program and competency pack to assist in your development.
  • There is an established mentorship programme and all new team members are assigned a Mentor.

Responsibilities

  • Support the Research Team to ultimately increase patient recruitment into clinical trials, promote the development of commercial research & contribute to high quality research.
  • You will be expected to interact with patients & families in relation to the requirements of clinical trials & be able to work without supervision in some areas.
  • You will be responsible for research data capture, data entry into databases/electronic case report forms, (treatment, observational/genetic), assisting with the set-up of new trials, maintaining study paper and electronic site files/documentation, processing protocol amendments, accurate documentation, identifying patients via MDT’s/screening notes, receiving consent, recruiting participants to research studies and supporting & monitoring research patients.
  • There will be a requirement to lead an observational/ genetic study following appropriate training & mentorship.

FAQs

What are the primary responsibilities of the Clinical Trial Assistant?

The primary responsibilities include supporting the Research Team with patient recruitment, data capture, data entry into electronic systems, assisting with trial setup, maintaining study documentation, processing protocol amendments, receiving consent, and monitoring research patients.

Where will the Clinical Trial Assistant primarily be based?

The Clinical Trial Assistant will primarily be based at Huddersfield Royal Infirmary, but may also work at Calderdale Royal Hospital as required.

What type of training will be provided to the successful candidate?

A full induction and training will be provided, including a structured training program and competency pack to assist in professional development.

Will the position require working in a multidisciplinary team?

Yes, the position requires working autonomously and as part of a research multidisciplinary team, collaborating with Research Midwives, Research Nurses, and Clinicians.

Is there an opportunity to develop clinical skills in this role?

Yes, there is potential to develop existing clinical skills, such as phlebotomy and vital signs collection, to support the Research Midwives/Nurses and Allied Health Professionals.

What is the working schedule for this position?

The CHFT research team operates Monday to Friday, 9-5, but there may be a future requirement for 7-day working.

Who can I contact for more information about the position?

For further details or informal visits, you can contact Naomi Greenhalgh, Clinical Research Nurse, at naomi.greenhalgh@cht.nhs.uk or call 01484 342905.

Will the Clinical Trial Assistant interact with patients and families?

Yes, the Clinical Trial Assistant will be expected to interact with patients and families regarding the requirements of clinical trials.

Is mentorship available for new team members?

Yes, there is an established mentorship program, and all new team members are assigned a Mentor to support their development.

Are there opportunities for career development in this role?

Yes, this position offers excellent opportunities to develop skills and expertise in research and contribute to the Trust's research portfolio.

Science & Healthcare
Industry
5001-10,000
Employees
2001
Founded Year

Mission & Purpose

Calderdale and Huddersfield NHS Foundation Trust (CHFT) offers a broad range of healthcare services, including acute, emergency, and elective care, across Calderdale and Huddersfield. Their mission is to provide high-quality, patient-centered care that improves health outcomes and ensures safety. Their purpose is to deliver excellent clinical services, enhance community well-being, and support continuous improvement and innovation in healthcare.