Job responsibilities 1. Clinical Research Management: Organise, arrange and maintain oversight of all studies in support of Principal Investigators, actively leading the team to fulfil delivery requirements and meet recruitment targets across commercial and academic studies. Ensure adherence to Good Clinical Practice (GCP) guidelines and research department protocols. Coordinate with the research team to manage research activities throughout the study lifecycle. 2. Participant Recruitment: Collaborate with GPs, practice staff, and healthcare professionals to identify and recruit eligible participants for research studies. Screen potential participants, explain study procedures, obtain informed consent, and ensure proper documentation of participant enrolment. Maintain accurate participant recruitment logs and communicate effectively with potential participants regarding study details and requirements. 3. Study Coordination: Serve as the primary point of contact for research participants, providing ongoing support, answering queries, and ensuring their engagement and compliance with study protocols. Collaborate with study teams as required to ensure the smooth execution of research activities. Coordinate study visits, follow-up assessments, and data collection, ensuring timely and accurate documentation. 4. Data Collection and Documentation: Adhere to standardised data collection procedures, ensuring accurate and consistent collection, recording, and management of research data. Adhere to data protection regulations and maintain strict participant confidentiality. Ensure high-quality data entry, validation, and quality control measures, minimising errors and discrepancies. Maintain detailed and organised study records, including source documents and case report forms. 5. Clinical Procedures: Perform clinical procedures within the scope of a registered nurse's practice, such as blood sampling, electrocardiograms (ECGs), vital signs measurements, and other research-specific assessments. Adhere to standard operating procedures and protocols to ensure participant safety, comfort, and well-being during procedures. Monitor for and manage any adverse events or complications, working closely with study Principal Investigators as required. 6. Compliance and Regulatory Affairs: Ensure compliance with relevant regulatory guidelines, NHS policies, local research governance frameworks, and ethical considerations. Maintain positive, productive, working relationships with Research Delivery Network colleagues, NIHR, Clinical Research Associates, and foster and support collaborations with external parties involved in research. 7. Quality Control and Assurance: Ensure the accuracy and integrity of study data. Monitor and/or respond to data queries to identify and address any deviations, non-compliance issues, or protocol violations. Participate in monitoring visits and inspections by external bodies, ensuring readiness and compliance with NHS and research standards. 8. Team Collaboration: Collaborate effectively with multidisciplinary research teams, including GPs, allied healthcare professionals and administrative staff. Contribute to team meetings, provide insights, and support colleagues in research-related activities. Foster a culture of teamwork, open communication, and shared learning to optimise individual and team professional development and research outcomes. 9. Continuous Professional Development: Stay updated with the latest requirements for your nursing role and qualifications for research, including advancements in primary care. Engage in professional development activities, including training programs, conferences, and workshops, to enhance research skills and maintain professional registration and competence.