Research Recruiter

West Suffolk Clinical Commissioning Group

Tetford

Remote

GBP 29,000 - 36,000

Full time

5 days ago
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Benefits offered by this job

NHS pension
Life insurance
Family benefits (adult dependents' and
Children's pension
Ill health benefits
Health service discounts
Health Cash Plan
Annual Leave

Job summary

Breckland Alliance Research, part of the NIHR-supported network, is expanding its team in the UK. We seek a full-time Research patient recruiter to identify and recruit participants for clinical trials, using SystmOne searches and rigorous pre-screening.

You will work with clinicians and the patient engagement team to inform consent, support participants, and ensure high-quality trial delivery while adhering to GCP standards.

Qualifications

  • Experience with SystmOne clinical system.
  • Strong data analysis and Excel skills.
  • Knowledge of medications and long-term conditions.
  • Excellent and empathetic communication to explain trials to patients.
  • Compassionate approach valuing patients, relatives and carers.
  • Experience working on clinical research.

Responsibilities

  • Create thorough SystmOne searches based on study criteria.
  • Identify and recruit eligible participants to studies.
  • Provide information to participants to facilitate informed consent.
  • Assess patient eligibility with clinicians and perform pre-screening.
  • Be primary contact for participants on a clinical study.
  • Identify recruitment barriers and inform PI/Research Manager with action plans.
  • Maintain accurate documentation of research activities in study records.
  • Follow local, network and sponsor policies to ensure GCP and governance compliance.
  • Maintain site and investigator files.

Skills

Data analysis
Excel
Communication
Compassionate care
Clinical research
SystmOne experience

Tools

SystmOne

Job description

About the Role

Due to expansion, Breckland Alliance Researchhas a fantastic opportunity for a Research patient recruiterto join our team on a full-time basis.

The main responsibilities of the role include:

  • Create thorough SystmOne searches based off study inclusion and exclusion criteria
  • Responsible for the identification of suitable participants; recruitment of eligible participants to studies and trials
  • Provide ongoing advice and information to participants about their participation in clinical research to facilitate effective informed consent, working closely with the patient engagement and communications coordinator
  • Work with the doctors, nurses and administrative teams in the assessment of patients’ eligibility for the research trials including thorough pre screening of patients medical records.
  • Act as primary point of contact for participants on a clinical study
  • Identify barriers to recruitment and ensure PI and Research Manager is aware of them; identify and implement action plans to remove these barriers
  • Maintain accurate documentation of research related activities in the study and surgery notes
  • Follow all local, network and sponsor policies and procedure to ensure you are working according to GCP and Research Governance standards for the clinical studies
  • Maintain the site and investigator files

For further information, please see job description attached.

About the Candidate

We are open to candidates with varying qualifications.As this is a new an exciting role we understand that many clinicians will have the skills and experience for this role.We would consider applicants from registered colleagues including but not limited to Pharmacy Technicians, Nurses, Research practitioners, Physician Assistants and Nursing Associates.

All applicants should have the following qualifications, registrations, skills and experience:
  • Experience of clinical system SystmOne
  • Data analysis and excellent excel knowledge
  • Medication and Long term condition knowledge
  • Exemplary communication skills to help patients to understand the value and reward of joining clinical trials.
  • Compassionate manner with an empathetic approach and demonstrable kindness in all aspects of your work. The successful candidate will value the dignity of our patients, their relatives and carers, as well as their colleagues at the practice
  • Experience working on clinical research
About Us

At Breckland Alliance, we have proudly received funding from the National Institute for Health and Social Care Research (NIHR) to become The Breckland and Norfolk Region Primary Care Commercial Research Delivery Centre (CRDC(PC)). We are part of the CRDC UK Network, which brings together 35 centres across primary, secondary and specialist care to strengthen the UK’s position as a global leader in commercial clinical research. In partnership with the pharmaceutical industry, the network provides a coordinated UK wide infrastructure for fast, reliable and consistent trial delivery at scale. It offers industry access to high-performing research sites and enables inclusive, decentralised trials, allowing more people from more communities across the NHS to take part in research.

Breckland Alliance Research works with Grove Surgery, School Lane Surgery and Watton Medical Practice. With a population of approximately 45,000 patients.

Some of the benefits for working with us include:

  • NHS pension scheme
  • Life insurance
  • Family benefits including an adult dependents and childrens pension
  • Ill health benefits
  • Health service discounts
  • Health Cash Plan -which includes cash towards dental care, optical care, gym memberships and additional reward schemes
  • Annual Leave: minimum 25 days FTE, with additional bank holidays
Disclosure and Barring Service Check

Please note this post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service to check for any previous criminal convictions.

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