About the Company 

Re:Cognition Health is a leading provider of clinical services specialising in cognitive impairment. We deliver expert clinical care to private patients and are one of the foremost providers of clinical trials in the world and deliver award winning medico-legal services. The Company is highly innovative, currently operating from four locations and has ambitious plans to expand geographically. We value people who are dedicated, hardworking and looking to contribute to the continued growth of the business.

The primary responsibility of all RCH SI/RMO’s is the safety, well-being and interests of our patients. The key responsibilities of the role are:

1. Working under the direct supervision of the Principal Investigator and Consultants on all SI/RMO responsibilities and delegated duties

2. Performing these responsibilities and duties in accordance with ICH, GCP,CQC, GMC and MHRA and company guidelines

3. Deliver services to our patients/subjects in line with our trial/service specifications:

• Conduct follow-up consultations focused on monitoring symptoms, treatment response, and side effects.

• Prescribe and manage patients/subjects dosing in line with PI/consultant instructions and clinical protocols.

• Review patients/subjects histories, investigation results, and ongoing care needs.

• Escalate complex cases or concerns to the PI/consultant, promptly.

• Provide clear, compassionate communication to patients/subjects regarding treatment plans and next steps.

• Demonstrate an accurate and comprehensive understanding of the informed consent process, for both trials and services

• Maintaining adequate control of study drug/private service drugs and appropriate records of drug disposition (primary responsibility of the site pharmacist).

• Ensure prompt reporting of serious and unexpected adverse events to the PI/Consultant

4. Participate in SI/RMO rota to ensure patients/subjects appointments and clinical needs are covered during the opening hours of RCH Centres – which may vary according to Company requirements.

5. To support occasional out of hours activity, to ensure patient safety is maintained.

6. Maintaining adequate records of patients/subjects participation in trials/services

8. Participate in internal training and CPD activities to maintain and enhance clinical skills via delegated trainings and RCH Academy.

9. Deliver services to our patients/subjects in line with good governance practices.

10. To perform other duties of an administrative nature appropriate to your position which may be required from time to time

The Candidate 

To be considered for our Sub-Investigator Clinical Trials/Resident Medical Officer role, you will have the following skills and experience:

Essential 

Applicants must be medically qualified, and registered with the GMC.

Applicants must have a minimum of 1 year experience, post qualifying, in the UK

Applicants must have experience of emergency medicine

Applicants must have experience of neurological conditions

Applicants must have experience of research in relevant clinical topics

Desirable 

Experience in working in clinical trials

Experience in delivering private services

Salary and Benefits:

Salary for role: £65,000 (full time). Part time role - 2 days, plus option to flex up

•Continuous professional development

•25 Days Annual Leave + Bank Holidays

•Private Health Insurance

•Life insurance

•Employee Assistance Program

•Pension Scheme

•Perkbox

•Free Mortgage Advisor Scheme

•Electric Vehicle Scheme

If you feel you have the skills for the role, please apply now!