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Clinical Research Practitioner

Medway NHS Foundation Trust

England

On-site

GBP 60,000 - 80,000

Full time

Yesterday
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Job summary

An established industry player in healthcare is seeking a dedicated individual to assist in managing research projects. This role involves supporting the setup and conduct of clinical trials, ensuring compliance with health research standards, and maintaining accurate documentation. The ideal candidate will possess strong communication and organisational skills, along with a foundational understanding of health research in the UK. Join a team that values your contributions and offers a dynamic environment where you can grow and develop your skills while making a meaningful impact in the healthcare sector.

Qualifications

  • Good level of education, preferably in Health Science or Nursing.
  • Experience in research pharma or similar environments is considered.

Responsibilities

  • Assist in managing research projects and recruitment targets.
  • Maintain accurate records and report any protocol deviations.

Skills

Prioritisation of workload
Written communication skills
Oral communication skills
Organisational skills
Interpersonal skills
Ability to develop new skills

Education

1st Degree/Diploma in Health Science
Relevant subject or experience in research

Job description

Detailed job description and main responsibilities

Will assist in the management of research projects providing the necessary support so that studies can be set up and conducted safely, efficiently according to the required standards & targets.


Assist in the delivery of recruitment targets in line with the contractual agreements, agreed timelines.


Open and manage allocated projects, set timescales and resolve problems. This includes management of the set-up process.


Take responsibility for all areas of practice relating to the conduct of clinical trials and research studies.


Maintain accurate records of portfolio activities.


Under supervision, report, address, help to resolve any breaches and protocol deviations. Report Adverse Events (AEs) using appropriate procedures, including the expedited reporting of Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs).


Prepare/assist with preparation of patient documentation for research-related treatment clinics, complete accurate records of patient care, maintain source data and Case Report Forms and all other trial documents in a manner conducive to audit.


Person specification

Qualifications

Essential criteria
  • Good level of education.
  • Preferably 1st Degree/Diploma in Health Science, Nursing or other relevant subject.
  • Alternatively, experience in research pharma or other health/research-related institution will be considered.
Knowledge

Essential criteria
  • Understanding of health research in the UK.
  • Knowledge of Research Governance Framework, Medicines for Human Use Regulations, Good Clinical Practice and the Health Research Authority (HRA).
Experience

Essential criteria
  • Experience in assisting/participating in a research trial or similar.
  • Experience of working in NHS setting or other research environment.
Skills

Essential criteria
  • Ability to prioritise workload and manage own time effectively.
  • Excellent written and oral communication skills.
  • Proven organisation skills.
  • Ability to develop new skills.
  • Excellent interpersonal skills.
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