Job Description

We are looking for a motivated and enthusiastic Assistant Clinical Research Practitioner to join our dynamic team in the Centre for Clinical Infection and Diagnostics Research (CIDR). This is a fantastic opportunity to contribute to cutting-edge research in infectious diseases, including faecal microbiota transplantation and microbiome-based therapies.



Coordinate research clinics and participant care across multiple clinical studies.



Assist in the recruitment, consent, and follow-up of participants in line with study protocols.



Perform clinical assessments (e.g. BP, temperature, urinalysis, venepuncture) and ensure timely reporting of adverse events.



Maintain accurate study documentation, site files, and databases including case report forms.



Manage sample collection, storage, and shipment to ensure data integrity and participant safety.



Support data collection and quality control processes, and assist with study set-up, monitoring, and close-out.



Communicate effectively with participants, clinical teams, and study sponsors.



You'll be joining a world-class infectious diseases research team within CIDR -- a nationally recognised leader in translational research. The Centre's focus includes diagnostics for acute infections, antimicrobial resistance, and clinical trials for novel therapies and vaccines. Our team actively leads research in faecal microbiota transplantation (FMT), including trials such as PROMISE, aiming to improve outcomes in patients with cirrhosis and other chronic conditions.

Clinical and Communication:

Deliver safe, participant-focused care while ensuring protocol compliance.



Assist with screening and identifying eligible patients for research studies.



Conduct follow-up assessments via phone or in person and communicate complex study-related information sensitively.



Support the participant journey by maintaining clear, compassionate, and professional communication.

Data and Study Administration:

Maintain clinical research files, databases, and logs in accordance with Good Clinical Practice (GCP).



Complete case report forms and coordinate data collection and monitoring visits.



Update recruitment trackers and ensure accurate data entry into Trust systems such as EDGE.

Leadership and Teamwork:

Collaborate with research nurses, doctors, laboratory staff, and administrative teams.



Provide guidance to junior or new team members.



Contribute to meetings, conferences, and study initiation events as needed.

Training and Development:

Take ownership of your learning and development, including meeting Care Certificate and Trust appraisal standards.



Stay updated on research protocols, amendments, and relevant SOPs.

Additional Duties:

Order study supplies, maintain inventory, and ensure smooth day-to-day operations.



Support archiving processes and site closeout procedures.



Contribute to Trust-wide initiatives including sustainability, equality, and safeguarding.