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Clinical Trials Sub Investigator (Research Physician), Winchester
Client:
Re:Cognition Health
Location:
Winchester, United Kingdom
Job Category:
Other
EU work permit required:
Yes
Job Reference:
d851fd1b80e5
Job Views:
4
Posted:
14.03.2025
Expiry Date:
28.04.2025
Job Description:
Re:Cognition Health (London based) is a pioneering brain and mind clinic that specializes in the treatment and care of people showing symptoms of cognitive impairment. Utilizing the latest progressive medical research and evidence-based treatments, we are passionate about transforming and optimizing cognitive performance through education and clinical excellence.
The Re:Cognition Health Clinics in London, Winchester, Surrey, Birmingham, Guildford, Plymouth, Bristol, and Washington DC are also major centers for international trials of disease-modifying and new symptomatic drugs for Alzheimer’s disease and other neurological conditions in adults and children. Our multi-disciplinary team works collaboratively to provide a full service, patient-centered approach.
We are seeking a Clinical Trials Sub Investigator for our Winchester clinical research site to support clinical trials investigating innovative treatments for mental health disorders. The ideal individual is a dedicated, hardworking individual with experience in cognitive disease and clinical research.
This is a full-time position. The candidate must be a GMC registered doctor. The successful candidate will be provided the opportunity to undertake the 4-year Pharmaceutical Medicine Specialty Training (PMST) to receive a CCT in pharmaceutical medicine from the Faculty of Pharmaceutical Medicine.
Role:
The primary responsibility of the sub-investigator is to ensure the well-being, safety, and interests of all participants at your center taking part in clinical trials. The Principal Investigator has overall responsibility for the conduct of the clinical trials and will delegate specific duties to an appropriately trained and qualified Sub-Investigator.
Key Objectives and Responsibilities:
1. Working under the direct supervision of the Principal Investigator to perform the clinical trials in accordance with ICH GCP (R2).
2. Ensure complete understanding of the clinical trial protocol(s) to provide complete information and explanation to potential participants, to obtain written informed consent.
3. Undertake and oversee the medical screening for potential participants, including ECGs, vitals, venepuncture, and lumbar puncture, to ensure they meet the entry requirements of each clinical trial protocol.
4. With the PI, consider the participant's eligibility for each clinical trial protocol, according to the specific inclusion and exclusion criteria, prior to randomization.
5. Perform ongoing follow-up assessments, including clinical examinations (physical/neurological examinations, ECGs, vital signs, bloods) and dosing procedures as appropriate to each study.
6. Review and evaluate Vital Signs, ECGs, and Laboratory test results for all studies, ensuring that any clinically significant abnormal results and/or changes from baseline are reported, and action taken to the Principal Investigator, Medical Monitor, and/or Sponsor contacts.
7. Represent Re:Cognition Health and the site during sponsor-led meetings, including pre-site selection, site initiation, and onsite monitoring visits, providing essential medical input.
8. Lead on the resus equipment checking and medical emergency scenario training at the site.
9. Provide support to the central recruitment team in the capacity of a research physician.
Ideal Candidate:
1. A medical doctor with at least 2 years of clinical experience (post-registration).
2. Must have completed foundation and core medical competencies.
3. GMC Registered with a License to Practice and comply with revalidation requirements.
4. Member of a suitable medical defence organization (e.g., MDU or MPS).
5. Experience of managing participant safety (eligibility, ongoing review/assessment) and management of Medical Emergencies.
6. Postgraduate membership qualification by exam MRCP or equivalent.
7. Valid Advanced Life Support (ALS) certificate from the Resuscitation Council (UK).
8. Previous Clinical Trial Experience.
9. Desire to progress to becoming a Principal Investigator.
Benefits:
* 25 Days Annual Leave + Bank Holidays
* Employee Assistance Program
* Free Mortgage Advisor Scheme
* Electric Vehicle Scheme
Salary: £65-67,500 per annum, depending on experience
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