Clinical Research Practitioner

South London and Maudsley NHS Foundation Trust

A unique opportunity has come up at our new Centre for Mental Health Research and Innovation (CMHRI) to work on clinical trials as a Clinical Research Practitioner.

South London and Maudsley NHS Foundation Trust (SLaM) is working in collaboration with Kings College London and COMPASS Pathways, a mental health care company dedicated to accelerating patient access to evidence-based innovation in mental health.

This pioneering collaboration will provide patient access to cutting edge research studies within the newly developed Clinical Research Unit at 5 Windsor Walk.

Main duties of the job

The post-holder will be responsible for a range of clinical, administrative, and supportive tasks essential for the smooth running of research activities. This includes performing clinical procedures, participant recruitment, data management, and maintaining the clinic environment to ensure safety and efficiency.

Job responsibilities

1. Clinical Procedures:
   • Conduct electrocardiograms (ECGs) following standard protocols.
   • Monitor and record patient vitals, ensuring accuracy and consistency.
   • Conduct urinalysis tests as per research study requirements.
2. Participant Recruitment and Phone Screenings:
   • Conduct phone screenings to assess potential participants' eligibility for research studies.
   • Explain study protocols, procedures, and requirements to prospective participants during phone screenings.
   • Recruit eligible participants, scheduling them for clinic visits and ensuring they receive necessary study information.
3. Data Management:
   • Accurately enter research data into electronic data capture systems.
   • Resolve data queries promptly, liaising with relevant teams to ensure data integrity.
   • Maintain accurate and up-to-date clinical records, ensuring confidentiality and compliance with data protection regulations.
4. Clinic Maintenance and Upkeep:
   • Ensure the clinic area is well-maintained, clean, and organized.
   • Conduct regular stock checks and replenish clinical supplies as needed.
   • Perform safety checks in the clinic environment, ensuring all equipment is functioning properly and reporting any issues.
5. Patient and Participant Support:
   • Provide a high standard of care to research participants, ensuring their safety and comfort.
   • Educate participants about the procedures and protocols of the research study.
   • Address participant queries and concerns, escalating complex issues to senior staff as necessary.
6. Compliance and Quality Assurance:
   • Adhere to all relevant clinical governance, research governance, and regulatory requirements.
   • Participate in quality assurance activities, including audits and inspections.
   • Work closely with the multidisciplinary team to support the delivery of research projects.
   • Attend team meetings and contribute to the continuous improvement of clinical research processes.

Person Specification Qualifications

• Evidence of continuous personal and professional development

Experience

• Strong organisational and data management skills
• Understanding of clinical research processes and Good Clinical Practice (GCP)
• Previous experience in a research environment
• Experience in handling biological blood samples
• Experience in participant recruitment and conducting phone screenings

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.

Compensation

£35,964 to £43,780 a year per annum including HCA

Contract

Fixed term

Duration

12 months

Working pattern

Full-time

Reference number

334-CLI-

Job location

Centre for Mental Health Research and Innovation (CMHRI)