Job summary We are excited to offer a permanent opportunity for a Band 6 Registered Research Midwife to join the Research Development and Innovation Team at Mersey and West Lancashire Teaching Hospitals NHS Trust (MWL). This is an excellent chance to contribute to cutting-edge research in a dynamic, multi-disciplinary environment. As part of our team, you will collaborate with Principal Investigators, Research Nurses, clinicians, and academic staff to deliver high-quality research projects. This role involves working across both Southport and Ormskirk District General Hospitals, with potential flexibility to work at other MWL sites such as Whiston and St. Helens Hospitals as needed. There will be a requirement to travel between sites to support research activities. We are looking for an organised, motivated individual with a passion for advancing research in maternity care. If you're proactive and thrive in a fast-paced setting, we encourage you to apply. Interview Date - To Be Confirmed Main duties of the job Assist in the setup, delivery, and management of both commercial and non-commercial research studies. Collaborate with research teams, including Principal Investigators and Research Nurses, to ensure studies are conducted to the highest standards. Provide exceptional care and support to research participants and, where appropriate, their families, ensuring a compassionate and professional approach. Manage a portfolio of research studies, overseeing day-to-day operations and delegating tasks to team members as required. Maintain accurate documentation and ensure compliance with regulatory standards throughout all research processes. We are looking for candidates with experience in a research role, ideally within a healthcare setting. You should have: Excellent interpersonal skills and the ability to work collaboratively in a multidisciplinary team. Strong organisational skills and the ability to manage a diverse workload and research portfolio. Clear, concise written and verbal communication skills. A methodical approach to your work, with an eye for detail. Flexibility to adapt to service needs and work across multiple sites as necessary This is predominantly a Monday to Friday role, though some flexibility may be required to meet the needs of the service. About us Mersey and West Lancashire Teaching Hospitals NHS Trust serves a population of over 600,000 with a workforce of over 9000 dedicated and skilled staff across 21 sites. We strongly believe that the communities we serve should all have access to Five Star Patient Care. Our services: Acute Care Providing emergency and maternity services at Whiston, Southport and Ormskirk hospitals, and medical and surgical specialties across all our sites. Primary Care Providing primary care services at Marshalls Cross Medical Centre situated in St Helens Hospital. Community Services Providing adult community services for St Helens and a wheelchair service in Chorley, South Ribble, and West Lancashire. Our inpatient unit at Newton Community Hospital is where patients needing acute hospital beds can continue rehabilitation, freeing up space for more unwell patients. We also provide urgent care at our Urgent Treatment Centre located in St Helens town centre. Specialist Regional Services We provide the Mersey Regional Burns & Plastic Surgery Unit at Whiston Hospital and the Spinal Injuries Unit at Southport Hospital to more than 4 million people across the whole of Merseyside, West Lancashire, Cheshire, Isle of Man and North Wales. Achievements: Rated Outstanding by CQC Inspection August 2018 Top 100 places to work in the NHS (NHS Employers & Health Service Journal) National Preceptorship Accreditation (2023) for Nursing & AHP Preceptorship Programme Date posted 09 January 2025 Pay scheme Agenda for change Band Band 6 Salary £37,338 to £44,962 a year Per Annum, Pro Rata Contract Permanent Working pattern Part-time Reference number 409-6861219 Job locations Ormskirk District General Hopsital Wigan Road Ormskirk L39 2AZ Job description Job responsibilities KEY DUTIES Knowledge of clinical research including issues on ethics, law, drug development and management in clinical issues. Management of clinical resources, equipment, and staff members. Partly responsible for submissions to research ethics committees. Always Maintaining overall standard of care for patients. Educational and developmental role. Ability to give advice on the organisation and management of research in progress. Liaison with sponsor companies and multi-disciplinary research teams. Good project management skills. To contribute to all aspects of the planning, conduct and reporting of all clinical trials within the research speciality. To be responsible for the day-to-day management of, patient recruitment to research studies. To work daily with minimal supervision as part of a research team. To ensure that all clinical research activity is ICH GCP compliant and conducted in accordance with agreed protocols. To maintain a high standard of patient care in line with Trust and R&D policies and protocols and in accordance with the UK Policy Framework for Health and Social Care Research. To prioritise research activity as necessary thus ensuring recruitment targets are met. To ensure that all data is collected and managed accurately. To co-ordinate all designate clinical research studies as directed by lead clinician to ensure recruitment targets are met. To identify, screen, interview patients and recruit them into the appropriate studies. To assist the principal investigator in the informed consent process, ensuring the subject in fully informed prior to participation to the study. To co-ordinate and carry out patient visits in accordance with study protocols, including co-ordinating special tests in other departments, collection of data, coding data entry and patient support. To carry out treatment procedures and treatment interventions according to pre-determined protocols, including venepuncture, venous cannulation, administering of intra-venous drugs and vital sign recording. To carry out the collection, processing, and shipping of biological specimens according to protocol requirements and follow up appropriately on alert values. To be involved in the education of patients and their various aspects of their disease. To ensure that patient safety is paramount in all procedures that take place for trial purposes. To report and record adverse and serious adverse events as per protocol. To ensure clinical and research document record keeping is completed accurately and efficiently in accordance with NMC and the Clinical Trials Regulations. To meet monthly with the senior nurse in R&D department for professional support and guidance. To have sufficient computer skills for the handling and management of computerised data. To keep up to date with relevant medical literature, developments in clinical research methodology, monitoring, and local regulatory and ethical requirements. To attend courses, conferences, and study days to remain up to date with all relevant aspects of clinical research. To attend monthly research network meetings. To understand the relevance of research to healthcare delivery and be able to identify research problems with the speciality. To develop the skills of other members of staff by identifying needs through observation and ensuring participation, practice, and relevant education. To participate in the education and development of student nurses. CLINICAL & PROFESSIONAL RESPONSIBILITIES It is anticipated that the individual post-holder will meet the following requirements of the post: Previous experience in the research speciality is desirable. More that 2-3 years post basic experience. The ability to work independently and prioritise own caseload. To possess computer skills. To have excellent interpersonal and communication skills. Effective time management skills. Competent in the skills of venepuncture and IV cannulation. PROFESSIONAL ACCOUNTABILITIES Compliance with GCP. Compliance with the law including Nursing Midwifery and Health Visiting Act 1979 and with the NMC Code of Conduct. Compliance with the Data Protection Act 1984 and the Computer Misuse Act 1990. Compliance with Trust, Directorate and LTC policies and protocols. Maintenance of personal and professional development. This job description is by no means exhaustive and is intended as a guide to the post holder. This specification may be reviewed in the future by the Clinician leading the study in collaboration with the R&D office. Job description Job responsibilities KEY DUTIES Knowledge of clinical research including issues on ethics, law, drug development and management in clinical issues. Management of clinical resources, equipment, and staff members. Partly responsible for submissions to research ethics committees. Always Maintaining overall standard of care for patients. Educational and developmental role. Ability to give advice on the organisation and management of research in progress. Liaison with sponsor companies and multi-disciplinary research teams. Good project management skills. To contribute to all aspects of the planning, conduct and reporting of all clinical trials within the research speciality. To be responsible for the day-to-day management of, patient recruitment to research studies. To work daily with minimal supervision as part of a research team. To ensure that all clinical research activity is ICH GCP compliant and conducted in accordance with agreed protocols. To maintain a high standard of patient care in line with Trust and R&D policies and protocols and in accordance with the UK Policy Framework for Health and Social Care Research. To prioritise research activity as necessary thus ensuring recruitment targets are met. To ensure that all data is collected and managed accurately. To co-ordinate all designate clinical research studies as directed by lead clinician to ensure recruitment targets are met. To identify, screen, interview patients and recruit them into the appropriate studies. To assist the principal investigator in the informed consent process, ensuring the subject in fully informed prior to participation to the study. To co-ordinate and carry out patient visits in accordance with study protocols, including co-ordinating special tests in other departments, collection of data, coding data entry and patient support. To carry out treatment procedures and treatment interventions according to pre-determined protocols, including venepuncture, venous cannulation, administering of intra-venous drugs and vital sign recording. To carry out the collection, processing, and shipping of biological specimens according to protocol requirements and follow up appropriately on alert values. To be involved in the education of patients and their various aspects of their disease. To ensure that patient safety is paramount in all procedures that take place for trial purposes. To report and record adverse and serious adverse events as per protocol. To ensure clinical and research document record keeping is completed accurately and efficiently in accordance with NMC and the Clinical Trials Regulations. To meet monthly with the senior nurse in R&D department for professional support and guidance. To have sufficient computer skills for the handling and management of computerised data. To keep up to date with relevant medical literature, developments in clinical research methodology, monitoring, and local regulatory and ethical requirements. To attend courses, conferences, and study days to remain up to date with all relevant aspects of clinical research. To attend monthly research network meetings. To understand the relevance of research to healthcare delivery and be able to identify research problems with the speciality. To develop the skills of other members of staff by identifying needs through observation and ensuring participation, practice, and relevant education. To participate in the education and development of student nurses. CLINICAL & PROFESSIONAL RESPONSIBILITIES It is anticipated that the individual post-holder will meet the following requirements of the post: Previous experience in the research speciality is desirable. More that 2-3 years post basic experience. The ability to work independently and prioritise own caseload. To possess computer skills. To have excellent interpersonal and communication skills. Effective time management skills. Competent in the skills of venepuncture and IV cannulation. PROFESSIONAL ACCOUNTABILITIES Compliance with GCP. Compliance with the law including Nursing Midwifery and Health Visiting Act 1979 and with the NMC Code of Conduct. Compliance with the Data Protection Act 1984 and the Computer Misuse Act 1990. Compliance with Trust, Directorate and LTC policies and protocols. Maintenance of personal and professional development. This job description is by no means exhaustive and is intended as a guide to the post holder. This specification may be reviewed in the future by the Clinician leading the study in collaboration with the R&D office. Person Specification Qualifications Essential Registered Midwife Degree or equivalent post basic studies Attendance at recent short courses and/or study days on research Desirable Post Basic study in speciality Masters level Degree Certificate in clinical research Knowledge & Experience Essential Previous experience in clinical research studies Experience of liaison with staff at all levels in the Health Service, Universities and Industry Experience of patient education and counselling, e.g. providing lifestyle advice Clinical experience / qualification in venepuncture, IV cannulation Supervision of students Knowledge of the principles and practice of clinical research and/or clinical trials Understanding of the role & responsibilities of a clinical research nurse Knowledge of ethical and quality standards applicable to clinical trials, including EW Directive on ICH GCP requirements Understanding of the relevance of research to health care delivery and the ability to demonstrate knowledge of the specific research subject Desirable Experience of co-ordinating clinical research studies Experience of leading the development of research projects (protocols and study documentation) and negotiating research funding Knowledge of the Health Service, R&D, the pharmaceutical industry partnership and relevant information services Skills in handling and management of computerised data (e.g. the abstraction and coding of medical data, computer data entry, statistical analysis, report generation and data validation) Skills Essential Ability to use a personal computer, (computer literacy and proficiency in MS Office / EDCL) Ability to work independently and prioritise own workload and to communicate effectively with all members of the multidisciplinary team Ability to meet tight deadlines and cope in a highly demanding environment Possession of tact and sensitivity to the needs of both patients and colleagues, including commitment to confidentiality Meticulous attention to detail and a high standard of accuracy, e/g/ in the capture and validation of clinical trial data Excellent and effective verbal and written communication skills Other Essential Skills in administration of research and project management Good communication, presentational training and interpersonal skills Desirable Skills required to evaluate and assist in developing new protocols Skills in the analysis and interpretation of data Person Specification Qualifications Essential Registered Midwife Degree or equivalent post basic studies Attendance at recent short courses and/or study days on research Desirable Post Basic study in speciality Masters level Degree Certificate in clinical research Knowledge & Experience Essential Previous experience in clinical research studies Experience of liaison with staff at all levels in the Health Service, Universities and Industry Experience of patient education and counselling, e.g. providing lifestyle advice Clinical experience / qualification in venepuncture, IV cannulation Supervision of students Knowledge of the principles and practice of clinical research and/or clinical trials Understanding of the role & responsibilities of a clinical research nurse Knowledge of ethical and quality standards applicable to clinical trials, including EW Directive on ICH GCP requirements Understanding of the relevance of research to health care delivery and the ability to demonstrate knowledge of the specific research subject Desirable Experience of co-ordinating clinical research studies Experience of leading the development of research projects (protocols and study documentation) and negotiating research funding Knowledge of the Health Service, R&D, the pharmaceutical industry partnership and relevant information services Skills in handling and management of computerised data (e.g. the abstraction and coding of medical data, computer data entry, statistical analysis, report generation and data validation) Skills Essential Ability to use a personal computer, (computer literacy and proficiency in MS Office / EDCL) Ability to work independently and prioritise own workload and to communicate effectively with all members of the multidisciplinary team Ability to meet tight deadlines and cope in a highly demanding environment Possession of tact and sensitivity to the needs of both patients and colleagues, including commitment to confidentiality Meticulous attention to detail and a high standard of accuracy, e/g/ in the capture and validation of clinical trial data Excellent and effective verbal and written communication skills Other Essential Skills in administration of research and project management Good communication, presentational training and interpersonal skills Desirable Skills required to evaluate and assist in developing new protocols Skills in the analysis and interpretation of data 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. UK Registration Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window). Additional information 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. UK Registration Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window). Employer details Employer name Mersey and West Lancashire Teaching Hospitals NHS Trust Address Ormskirk District General Hopsital Wigan Road Ormskirk L39 2AZ Employer's website https://www.merseywestlancs.nhs.uk/ (Opens in a new tab)