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Acting as patient and participant advocate at all times, the post holder will be expected to organize study related care for a range of clinical research facility studies. They will identify strategies to find and assist in the enrolment of research participants. The post-holder will perform a range of clinical assessments in line with accepted standards of practice and perform basic laboratory techniques. They will communicate effectively with the study and clinical teams to ensure good participant experience and adherence to study protocols. The post holder will be responsible for case report form completion, site file management and maintenance of databases. They will be responsible for ordering study supplies. The post holder will ensure the well-being of participants by adhering to relevant regulations and local Standard Operating Procedures (SOPs) including Good Clinical Practice (GCP), Medicines for Human Use (Clinical Trials) Regulations, Research Governance Framework for Health and Social Care and the Human Tissue Act.
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.
Are you a dynamic, patient-centered, and self-motivated individual looking for a new and exciting challenge?
The CRF is seeking to appoint a highly motivated person to join as an Assistant Clinical Research Practitioner. The post holder will work across various CRF studies, with a particular focus on our women's health portfolio. The ideal candidate will have some experience working in clinical research already and have either pre-existing basic laboratory skills or clinical skills.
The post will be initially created as an 12 month fixed term contract with a possibility for extension depending on funding. Secondments from internal candidates are welcome.
- Provide excellent customer care skills to ensure patients and participants come first.
- Work within relevant regulations and ICH GCP (International Conference on Harmonisation and Good Clinical Practice) ensuring that the study protocol is adhered to at all times.
- Co-ordinate research clinics and co-ordinate a portfolio of studies in conjunction with team members. This involves planning and organizing clinical study related care or tests in accordance with approved study protocols or departmental standard operating procedures.
- Perform and record a range of clinical assessments in line with personal competencies and as stipulated in approved study protocols including blood pressure, temperature, respirations, questionnaires, urinalysis, weight and height, and report abnormalities or changes appropriately.
- Perform tasks requiring clinical and laboratory skills, including phlebotomy, venepuncture, biological sample preparation within clinical area and laboratories as stipulated in approved protocols and laboratory manuals.
- Responsible for ensuring safe and appropriate storage, shipment and documentation of specimens.
- Communicate on a regular basis with senior medical staff, nursing, pharmacy, radiology, and pathology and laboratory staff.
- Update participant study and medical records to accurately document study related activity and procedures.
Acting as patient and participant advocate at all times, the post holder will be expected to organize study related care for a range of clinical research facility studies. They will identify strategies to find and assist in the enrolment of research participants. The post-holder will perform a range of clinical assessments in line with accepted standards of practice and perform basic laboratory techniques. They will communicate effectively with the study and clinical teams to ensure good participant experience and adherence to study protocols. The post holder will be responsible for case report form completion, site file management and maintenance of databases. They will be responsible for ordering study supplies. The post holder will ensure the well-being of participants by adhering to relevant regulations and local Standard Operating Procedures (SOPs) including Good Clinical Practice (GCP), Medicines for Human Use (Clinical Trials) Regulations, Research Governance Framework for Health and Social Care and the Human Tissue Act.
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.
Are you a dynamic, patient-centered, and self-motivated individual looking for a new and exciting challenge?
The CRF is seeking to appoint a highly motivated person to join as an Assistant Clinical Research Practitioner. The post holder will work across various CRF studies, with a particular focus on our women's health portfolio. The ideal candidate will have some experience working in clinical research already and have either pre-existing basic laboratory skills or clinical skills.
The post will be initially created as an 12 month fixed term contract with a possibility for extension depending on funding. Secondments from internal candidates are welcome.
- Provide excellent customer care skills to ensure patients and participants come first.
- Work within relevant regulations and ICH GCP (International Conference on Harmonisation and Good Clinical Practice) ensuring that the study protocol is adhered to at all times.
- Co-ordinate research clinics and co-ordinate a portfolio of studies in conjunction with team members. This involves planning and organizing clinical study related care or tests in accordance with approved study protocols or departmental standard operating procedures.
- Perform and record a range of clinical assessments in line with personal competencies and as stipulated in approved study protocols including blood pressure, temperature, respirations, questionnaires, urinalysis, weight and height, and report abnormalities or changes appropriately.
- Perform tasks requiring clinical and laboratory skills, including phlebotomy, venepuncture, biological sample preparation within clinical area and laboratories as stipulated in approved protocols and laboratory manuals.
- Responsible for ensuring safe and appropriate storage, shipment and documentation of specimens.
- Communicate on a regular basis with senior medical staff, nursing, pharmacy, radiology, and pathology and laboratory staff.
- Update participant study and medical records to accurately document study related activity and procedures.
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