Key responsibilities

·        Work closely with the Principal Investigator and Clinical Trials Team to manage the day-to-day activities of clinical trials.

·        Assist with problem-solving, communication and protocol management.

·        Build strong, professional relationships with patients participating in clinical trials.

·        Conduct trial activities in accordance with GCP guidelines, study protocols and regulatory requirements.

·        Assist with obtaining, documenting and maintaining informed consent.

·        Complete accurate and timely data entry, data queries and quality assurance checks.

·        Liaise with Clinical Research Associates and Sponsor Representatives.

·        Monitor, document and proactively follow up adverse events in accordance with study requirements.

·        Collect, process, label, handle and store clinical samples in accordance with trial protocols.

·        Coordinate and manage the logistics of study visits.

·        Maintain accurate and complete study records and documentation.

·        Maintain Investigator Site Files within SiteDocs – full training will be provided.

·        Maintain patient confidentiality and privacy at all times.

·        Assist the broader Clinical Trials Team to ensure studies remain organised, compliant and on schedule.

About you

·        Nursing qualifications or a degree in science, health science or another relevant healthcare discipline.

·        Previous experience working within a clinical trials or clinical research environment.

·        Knowledge and understanding of Good Clinical Practice (GCP).

·        A strong understanding of the importance of patient confidentiality, privacy and ethical clinical research.

·        Excellent verbal and written communication skills.

·        Strong interpersonal skills and the ability to develop positive relationships with patients, colleagues, investigators and sponsors.

·        Excellent attention to detail and a proactive approach to your work.

·        Strong organisational and time-management skills, with the ability to manage competing priorities and meet deadlines.

·        The ability to work independently while also being a collaborative and supportive team member.

·        Experience with Electronic Data Capture (EDC) systems, such as iMedidata RAVE, InForm or similar, would be highly desirable.

·        A professional, approachable and positive attitude.

Key responsibilities

·        Work closely with the Principal Investigator and Clinical Trials Team to manage the day-to-day activities of clinical trials.

·        Assist with problem-solving, communication and protocol management.

·        Build strong, professional relationships with patients participating in clinical trials.

·        Conduct trial activities in accordance with GCP guidelines, study protocols and regulatory requirements.

·        Assist with obtaining, documenting and maintaining informed consent.

·        Complete accurate and timely data entry, data queries and quality assurance checks.

·        Liaise with Clinical Research Associates and Sponsor Representatives.

·        Monitor, document and proactively follow up adverse events in accordance with study requirements.

·        Collect, process, label, handle and store clinical samples in accordance with trial protocols.

·        Coordinate and manage the logistics of study visits.

·        Maintain accurate and complete study records and documentation.

·        Maintain Investigator Site Files within SiteDocs – full training will be provided.

·        Maintain patient confidentiality and privacy at all times.

·        Assist the broader Clinical Trials Team to ensure studies remain organised, compliant and on schedule.

About you

·        Nursing qualifications or a degree in science, health science or another relevant healthcare discipline.

·        Previous experience working within a clinical trials or clinical research environment.

·        Knowledge and understanding of Good Clinical Practice (GCP).

·        A strong understanding of the importance of patient confidentiality, privacy and ethical clinical research.

·        Excellent verbal and written communication skills.

·        Strong interpersonal skills and the ability to develop positive relationships with patients, colleagues, investigators and sponsors.

·        Excellent attention to detail and a proactive approach to your work.

·        Strong organisational and time-management skills, with the ability to manage competing priorities and meet deadlines.

·        The ability to work independently while also being a collaborative and supportive team member.

·        Experience with Electronic Data Capture (EDC) systems, such as iMedidata RAVE, InForm or similar, would be highly desirable.

·        A professional, approachable and positive attitude.