FAQs
What specific responsibilities does the Clinical Trial Practitioner/Research Nurse have?
The Clinical Trial Practitioner/Research Nurse is responsible for coordinating and managing a clinical research portfolio, educating patients and colleagues, collecting and preparing biological samples, collecting trial data, monitoring side effects, and developing specialized skills related to clinical trials.
What types of clinical trials will I be working on?
You will be coordinating and conducting in-house, national, and international phase II and III clinical trials in hematological malignancies.
Will I be working independently or as part of a team?
You will be part of a multi-disciplinary team and will have autonomy in your role, allowing for collaboration as well as independent decision-making.
Is training available for this position?
Yes, the role includes the opportunity to develop specialized skills and knowledge relating to the conduct of clinical trials and to provide mentorship to data managers and clinical trial practitioners.
How will I support patients during their involvement in clinical trials?
You will act as a primary point of contact for patients, educating them and their families about clinical trials, including objectives, treatment schedules, side effects, and follow-up plans.
What measures are in place to ensure patient safety?
You will take personal responsibility for promoting a safe environment, identifying areas of risk, and following the incident reporting policy and procedure.
What kind of support will I receive from management?
You will receive support from the Clinical Trials Manager and be expected to provide cross-cover for other team members, facilitating a collaborative team environment.
Are there any requirements for critical appraisal skills?
Yes, you will be expected to apply critical appraisal skills in evaluating research protocols as part of your responsibilities.
Is previous experience in clinical trials necessary for this role?
Although previous experience in clinical trials is beneficial, what is more important is your ability to develop specialized knowledge and skills relating to the conduct of clinical trials.
How can I get more information about the position or arrange an informal visit?
For further details or informal visits, you can contact Ms. Tebereh Mesfin, the Senior Clinical Trial Practitioner Lead for Myeloma, at Tebereh.mesfin@nhs.net.