Clinical Research Nurse / Clinical Research Practitioner

Clinical Research Nurse / Clinical Research Practitioner We are looking for an enthusiastic and motivated Clinical Research Nurse / Clinical Research Practitioner to join our established Research Team and support the delivery of high-quality clinical research within primary care. With over 30 years experience delivering commercial research, our practice has a strong reputation for supporting clinical trials and providing patients with opportunities to take part in innovative research that helps shape the future of healthcare. This is an exciting opportunity for someone passionate about improving patient care through research. Working with patients, healthcare professionals and external research partners, you will support a diverse portfolio of studies across areas including diabetes, cardiovascular, respiratory, neurological, vaccines, mental health and community-based care. As part of a supportive multidisciplinary team, you will help identify and recruit participants, deliver study visits, support patients throughout their research journey, collect clinical data and ensure studies are delivered safely in line with Good Clinical Practice (GCP) and regulatory requirements. You will join a forward‑thinking practice that values innovation, teamwork and continuous improvement, with opportunities to develop your research skills and contribute to meaningful research outcomes. Main duties of the job The successful candidate will work as part of our Research Team to support the delivery of a range of clinical studies within a primary care setting. The role will involve supporting participants throughout their research journey, from identifying suitable patients and supporting recruitment, through to conducting study visits, completing clinical assessments, collecting samples where required and ensuring accurate recording of research data. You will work closely with the Senior Clinical Research Nurse, Clinical Research GPs and wider healthcare team to coordinate study activity, support participant safety and maintain high standards of care and compliance. The post holder will manage their own workload across multiple studies, communicate with patients, healthcare professionals and research partners, and contribute to the smooth running and ongoing development of the practices research portfolio. This role offers an opportunity to develop within a well‑established research environment, working on a variety of studies that contribute to improving patient care and advancing healthcare knowledge. About us Rowden Medical Partnership is a forward‑thinking GP practice committed to providing high‑quality, patient‑centred care to our local community. We are a large, established practice with a strong focus on teamwork, innovation and continuous improvement. Our Research Team has over 30 years experience delivering commercial research and plays an important role in providing patients with opportunities to participate in clinical studies that support the development of future treatments and healthcare services. We pride ourselves on creating a supportive and collaborative working environment where staff are encouraged to develop their skills, share ideas and contribute to improving the care we provide. Our multidisciplinary teams work closely together, valuing open communication, professionalism and a positive approach to change. As part of Rowden Medical Partnership, you will be joining a friendly and dedicated team that values the contribution of every member of staff. We are committed to supporting staff wellbeing, learning and development, while maintaining high standards for our patients and our colleagues. This is an exciting time to join our practice as we continue to develop our services, embrace new opportunities and build on our strong reputation within primary care and clinical research. Job responsibilities Job Description Job Title: Clinical Research Nurse / Clinical Research Practitioner Reports to: Senior Clinical Research NurseAccountable to: Clinical Research Lead Job Summary The post holder will work as part of the Research Team to support the delivery of high‑quality clinical research within Rowden Medical Partnership. They will contribute to the successful delivery of a portfolio of clinical studies across a range of specialities, including diabetes, cardiovascular, respiratory, neurological, vaccines, mental health and community‑based care. The post holder will support participants throughout their research journey, ensuring safe, compassionate and effective care in line with approved study protocols, Good Clinical Practice (GCP), research governance requirements and practice procedures. The role will involve identifying and recruiting eligible participants, conducting study visits, supporting clinical assessments, collecting samples where required, maintaining accurate research documentation and contributing to the successful delivery of research studies. Key Responsibilities Participant Care and Study Delivery * Support the set‑up and delivery of clinical research studies. * Identify, screen and recruit suitable participants using approved methods. * Conduct study visits in accordance with research protocols and delegated responsibilities. * Provide information, advice and support to participants and their families throughout their involvement in research. * Coordinate participant appointments, follow‑up activities and study requirements. * Liaise with GPs, healthcare professionals and external organisations to support safe participant care. Research Coordination and Data Management * Support multiple research studies and manage delegated study tasks. * Maintain accurate and timely research records, source documentation and electronic databases. * Ensure data collection is completed in line with study protocols, confidentiality requirements and regulatory standards. * Support monitoring visits, audits and inspections when required. * Assist with study‑related administration, sample processing and logistics. Clinical Responsibilities * Undertake clinical procedures appropriate to the role and level of competence, including sample collection where required. * Ensure infection prevention and control procedures are followed. * Maintain oversight of study equipment, medication and supplies where applicable. * Recognise and escalates participant safety concerns, protocol deviations, risks or issues affecting study delivery. Communication and Team Working * Work collaboratively with the Research Team, GPs, healthcare colleagues, patients and external research partners. * Provide regular updates regarding recruitment activity, study progress and outstanding actions. * Attend relevant meetings and contribute to the development of research services. * Promote research opportunities amongst clinicians, patients and the wider practice team. Professional Development and Governance * Maintain current knowledge of research governance, ethics and regulatory requirements. * Complete Good Clinical Practice (GCP) training and study‑specific training as required. * Participate in appraisal and continuing professional development activities. * Work in accordance with practice policies, NHS guidance, research regulations and confidentiality requirements. General Responsibilities The post holder will: * Maintain high standards of professionalism, confidentiality and patient‑centred care. * Support equality, diversity and inclusion within the workplace. * Contribute to quality improvement and effective team working. * Take responsibility for managing their own workload and maintaining professional standards. Person Specification * Registered Nurse qualification or completion of Clinical Research Practitioner competencies. * Experience of working in a clinical or patient‑facing healthcare environment. * Excellent communication and organisational skills. * Ability to work independently and as part of a multidisciplinary team. * Ability to manage competing priorities and work to deadlines. * Experience using electronic systems and Microsoft Office applications. * Experience working within a research environment. * Current Good Clinical Practice (GCP) certification. * Experience using SystmOne or other electronic patient record systems. * Experience of clinical procedures including venepuncture. * Experience supporting monitoring visits, audits or inspections. Person Specification Qualifications * Diploma / degree in nursing or completed Clinical Research Practitioner competencies Experience * Experience of working in a clinical or patient facing environment. * Proven experience of working to deadlines. * Proven experience of dealing with a busy workload. * Proven experience of competencies of IT systems including Microsoft Office applications * Experience of data management. * Experience in a research setting. * Current Good Clinical Practice (GCP) certification. * Experience using SystmOne. * Experience preparing documentation for monitoring visits, audits or inspections. Knowledge, Skills and Abilities * Knowledge/understanding of healthcare environments * Awareness and respect for confidentiality * Ability to work collaboratively within a multidisciplinary team. * Ability to communicate concerns and escalates issues appropriately. * Ability to work in a changing environment * Able to develop networks and learn from others * Ability to self‑reflect * Confident with Excel and Word * Experience of using electronic patient record systems * Proactive and able to work on own initiative * Ability to organise and prioritise own workload * Team player * Ability to remain calm and professional under pressure * Ability to delegate, where appropriate * Knowledge of the commercial and academic research environment * Medical knowledge/terminology * Knowledge of clinical governance. * Knowledge of information governance * Ability to troubleshoot effectively. 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. J-18808-Ljbffr