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Please refer to the attached job description and person specification which outlines the full and detailed responsibilities of this role. More information can be gained from contacting us on the details below.
We are seeking an experienced and dynamic clinical research practitioner to join our enthusiastic, friendly, and motivated multidisciplinary team within the NIHR Wolf Clinical Research Facility. The delivery of excellent care to children and young people receiving care through the clinical research pathway is central to this role. Applicants should have good experience in working within the NHS, a strong clinical background and a desire and willingness to learn and develop others. Candidates must demonstrate excellent communication and interpersonal skills, and have the ability and initiative to work independently and manage a patient caseload across a variety of research studies.
The post holder will be expected to manage a caseload of patients and have the duty of care in supporting them and their families throughout their participation in clinical trials. The role will include identifying suitable patients for clinical trials and work autonomously within professional practice guidelines and within the Research Governance Framework.
The post-holder will be allocated to support/lead a selection of trials and studies. The successful candidate will undertake clinical, laboratory and study management duties while ensuring patient safety and complying to Good Clinical Practice (GCP) Guidelines.
Candidates who have initiative, effective communication, and team work skills and clinical research experience are encouraged to apply.
Example of duties include but not limited to:
Clinical: phlebotomy, taking observations, recording ECGs and cannulation
Laboratory: processing, storing and shipping samples, leading on study feasibility reviews and supporting the department to meet laboratory compliance.
Study management: co-lead/lead on portfolio of trials, completing eCRF/CRFs, data query resolution, ISF maintenance, coordinating patient visits and trial assessment activities, reporting of AE/SAEs, liaising with internal and external CRA/sponsors/R&D, attending Study Initiation Visits, and hosting Monitoring Visits.
Please refer to the attached job description and person specification which outlines the full and detailed responsibilities of this role. More information can be gained from contacting us on the details below.
We are seeking an experienced and dynamic clinical research practitioner to join our enthusiastic, friendly, and motivated multidisciplinary team within the NIHR Wolf Clinical Research Facility. The delivery of excellent care to children and young people receiving care through the clinical research pathway is central to this role. Applicants should have good experience in working within the NHS, a strong clinical background and a desire and willingness to learn and develop others. Candidates must demonstrate excellent communication and interpersonal skills, and have the ability and initiative to work independently and manage a patient caseload across a variety of research studies.
The post holder will be expected to manage a caseload of patients and have the duty of care in supporting them and their families throughout their participation in clinical trials. The role will include identifying suitable patients for clinical trials and work autonomously within professional practice guidelines and within the Research Governance Framework.
The post-holder will be allocated to support/lead a selection of trials and studies. The successful candidate will undertake clinical, laboratory and study management duties while ensuring patient safety and complying to Good Clinical Practice (GCP) Guidelines.
Candidates who have initiative, effective communication, and team work skills and clinical research experience are encouraged to apply.
Example of duties include but not limited to:
Clinical: phlebotomy, taking observations, recording ECGs and cannulation
Laboratory: processing, storing and shipping samples, leading on study feasibility reviews and supporting the department to meet laboratory compliance.
Study management: co-lead/lead on portfolio of trials, completing eCRF/CRFs, data query resolution, ISF maintenance, coordinating patient visits and trial assessment activities, reporting of AE/SAEs, liaising with internal and external CRA/sponsors/R&D, attending Study Initiation Visits, and hosting Monitoring Visits.
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