Job summary
Clinical Research Assistant
Department Research & Development
Band 3 £22,816- £24,336 per annum, pro rata if part-time.
Hours: 37.5 hours per week, all MKUH roles will be considered for flexible working
This is an exciting opportunity for applicants with a minimum of 2 A-Levels/NVQ level 3 or equivalent to work within a busy research department with a portfolio of studies and clinical trials covering a range of conditions. These are NIHR supported studies both commercial and non-commercial. The post holder may be expected to interact with patients and their families in relation to the requirements of the study and be able to work without supervision in some areas. Prior experience is desirable though not essential. The post holders will learn about all aspects of clinical research with a focus on data and documentation and patient care including communication, obtaining, and processing biological samples and organising appointments and investigations. The position will have a Maternity and Reproductive Health focus as well as different specialties from Emergency Medicine to Cardiology, Oncology, Orthopaedics, MSK, Dermatology etc.
The post holder will also have excellent communication and interpersonal skills, good IT skills and knowledge of Excel, possess good timekeeping, prioritisation skills and be willing to learn and develop within the role.
Interview date: 11.01.2024
Main duties of the job
The post holder will provide assistance in all aspects of administration of clinical trial delivery and carry out allocated tasks that are related to the delivery of and day to day running of clinical trials.
Candidates with experience in healthcare settings are preferred for the role.
About us
You can expect a warm welcome at Milton Keynes University Hospital, our staff are friendly and welcoming. We listen to each other and work together to embed our Trusts values and behaviours. At MKUH we appreciate our staff and reward them with an outstanding benefits package including:
- Free on-site parking
- Free tea and coffee
- Great flexible workingopportunities
- Discounted gym membership
- Lease car scheme
- Generous annual leave and pension scheme
- On site nursery (chargeable)
- Extensive staff health and well-being programme
Milton Keynes University Hospital NHS Foundation Trust, in partnership with the University of Buckingham, is a University Teaching Hospital; we conduct research and teaching on site to improve the care of our patients. The hospital is undergoing significant investment, and we are proud to be rated good by the CQC. Visit our website to catch up on our latest news.
MKUH is committed to equal opportunities and improving the working lives of our staff and as such we offer a range of flexible working practices. We promote an inclusive workforce and encourage applications from applicants from all backgrounds.
We reserve the right to expire vacancies prior to the advertised closing date once a sufficient number of applications have been received.
MKUH uses identification scanning technology to confirm the authenticity of documents; all prospective employees of MKUH will have their original documents verified using this technology.
Job description
Job responsibilities
Administration
- Recording of clinical trial data onto case report forms (paper or electronic), checking for missing data and liaising with the research nurse to ensure that appropriate tests are carried out as per protocol requirements.
- Take action to obtain, or correct missing data (resolve data queries) while maintaining confidentiality and retrospectively gather information on previously treated patients.
Research practice
- To deal sensitively and in a professional manner with patients in person and on the telephone when dealing with queries and booking appointments.
- To adhere to the recommendations for the Control of Substances Hazardous to Health (COSHH) and risk assessments appropriate to the clinical area.
Professional Development
- To participate in the Trusts Individual Performance Review process and demonstrate commitment to on-going professional development by working towards the objectives agreed within an annual Personal Development Plan.
General
- To have responsibility for the Health, Safety and Welfare of self and others and to comply at all times with the requirement of the Health and Safety Regulations.
- To ensure confidentiality at all times, only releasing confidential information obtained during the course of employment to those acting in an official capacity in accordance with the provisions of the Data Protection Act and its amendments.
Please refer to the attached Job Description for more details on the role and responsibilities.
Job description
Job responsibilities
Administration
- Recording of clinical trial data onto case report forms (paper or electronic), checking for missing data and liaising with the research nurse to ensure that appropriate tests are carried out as per protocol requirements.
- Take action to obtain, or correct missing data (resolve data queries) while maintaining confidentiality and retrospectively gather information on previously treated patients.
Research practice
- To deal sensitively and in a professional manner with patients in person and on the telephone when dealing with queries and booking appointments.
- To adhere to the recommendations for the Control of Substances Hazardous to Health (COSHH) and risk assessments appropriate to the clinical area.
Professional Development
- To participate in the Trusts Individual Performance Review process and demonstrate commitment to on-going professional development by working towards the objectives agreed within an annual Personal Development Plan.
General
- To have responsibility for the Health, Safety and Welfare of self and others and to comply at all times with the requirement of the Health and Safety Regulations.
- To ensure confidentiality at all times, only releasing confidential information obtained during the course of employment to those acting in an official capacity in accordance with the provisions of the Data Protection Act and its amendments.
Please refer to the attached Job Description for more details on the role and responsibilities.
Person Specification
Qualifications and knowledge
Essential
- Minimum 2 A-levels/ NVQ level 3 or equivalent.
- Good verbal and written. communication skills.
- Computer literate with experience of Microsoft Office, including Access, Word and Excel.
Experience
Essential
- Experience in the handling and management of complex computer databases.
- Experience of working within a team environment.
Desirable
- Experience of working within a clinical trial setting.
- Experience in coordinating and managing the collection of research data.
Skills
Essential
- Capable of working on own initiative to problem solve.
- Good time management and a flexible willing attitude to working in a multi-disciplinary team.
- Good organisation and communication skills.
- Excellent attention to detail, methodical with high standards of accuracy.
- Ability to generate reports and extract information from a database.
- Good level of manual dexterity.
Desirable
- An understanding of medical terminology.
Personal and people development
Essential
- Demonstrable commitment to personal and professional development.
- The desire to educate others within the department and share best practice.
- Flexible approach.
- Smart Appearance.
- Good health/attendance records.
Communication
Essential
- Good communication and interpersonal skills, enthusiasm and a willingness to work closely and co-operatively with others.
Desirable
- Good presentation skills.
Specific requirements
Essential
- Able to perform the duties of the post with reasonable aids and adaptations.
Person Specification
Qualifications and knowledge
Essential
- Minimum 2 A-levels/ NVQ level 3 or equivalent.
- Good verbal and written. communication skills.
- Computer literate with experience of Microsoft Office, including Access, Word and Excel.
Experience
Essential
- Experience in the handling and management of complex computer databases.
- Experience of working within a team environment.
Desirable
- Experience of working within a clinical trial setting.
- Experience in coordinating and managing the collection of research data.
Skills
Essential
- Capable of working on own initiative to problem solve.
- Good time management and a flexible willing attitude to working in a multi-disciplinary team.
- Good organisation and communication skills.
- Excellent attention to detail, methodical with high standards of accuracy.
- Ability to generate reports and extract information from a database.
- Good level of manual dexterity.
Desirable
- An understanding of medical terminology.
Personal and people development
Essential
- Demonstrable commitment to personal and professional development.
- The desire to educate others within the department and share best practice.
- Flexible approach.
- Smart Appearance.
- Good health/attendance records.
Communication
Essential
- Good communication and interpersonal skills, enthusiasm and a willingness to work closely and co-operatively with others.
Desirable
- Good presentation skills.
Specific requirements
Essential
- Able to perform the duties of the post with reasonable aids and adaptations.
Disclosure and Barring Service Check
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 (formerly known as CRB) to check for any previous criminal convictions.
